Change Notice
 
 
Change Notice No.
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CN/17/12
Addition of pore size rating of different membrane layers (used in multilayered products) to respective Certificate of Quality (CoQ) and Product Package Label
CN/17/11
New printing design of packaging box for mdi Pre-sterilized Membrane Disc Filters
CN/17/10
Addition of water wetted Bubble Point Test Specification to the Certificate of Quality (CoQ) of 0.45 μm Polyethersulfone (PES) Membrane Cartridge and Capsule Filters of size 10"
CN/17/09
Improved Diluent Transfer Needle Assembly of mdi Stericheck: Closed Sterility Test System
CN/17/08
New printing design of packaging box formdi Funnel
CN/17/07
Addition of Bacterial Endotoxin and Cytotoxicity in Certificate of Quality formdi Hydrophilic PVDF Membrane Filters
CN/17/06
New printing design of packaging box formdi Glassfiber Disc Filters and Transfer Membranes
CN/17/05
Change in Lot numbering system and product package label of mdi pre-sterilized Centrifugal Filters and Vacufil
CN/17/04
Changes related to product catalog number, product lot number and certificate of quality of mdiAseptic Sampling System
CN/17/03
Change in specifications of Maximum Operating Temperature for mdi AseptiSure TH Hydrophobic PTFE Membrane Cartridge Filters.
CN/17/02
Improved design of of mdi Funnel (Funnel Base).
CN/17/01
Rationalization of product catalog number of mdi Centrifugal Filters.
CN/16/15
Improved product package label (with QR code) for mdi products.
CN/16/14
New design of vent/drain valves of mdi Large Capsule Filters
CN/16/13
Improved design of end connection type Female Luer Lock of mdi Capsule Filters
CN/16/12
Redefining product expiry date/shelf life of EO Sterilized Capsule Filters
CN/16/11
Change in Lot numbering system of mdi pre-sterilized Syringe Filters (All types)
CN/16/10
New printing design of packaging box for mdi Stericheck: Closed Sterility Test System
CN/16/09
Rationalization of product catalog number of mdi Stericheck SVP Dilutor
CN/16/08
Improved design of Inlet/Outlet connection type Female Luer Lock of mdi Capsule Filters
CN/16/07
Improved design of Protective Cap for Inlet/Outlet connection and Vent/Drain valve of mdi Capsule Filters
CN/16/06
New printing design of packaging box for mdi Disc Filters and Filter Media Strips
CN/16/05
Assigning Trade Names to products
CN/16/04
Change in Certificate of Quality for mdi Stericheck: Closed Sterility Test System
CN/16/01
Inclusion of Bubble Point Specification with 50% Isopropyl alcohol/water solution in Certificate of Quality (COQ) for Polyethersulfone Membrane Inline Filters
CN/16/03
Modification in identification on mdi Capsule Filters
CN/16/02
Rationalization of standard pack size of Inline Filters and Inline Vent Filters
CN/15/14
New printing design of packaging box for mdi Pre-sterilized Membrane Disc Filters
CN/15/12
New printing design of packaging box for mdi Large Capsule Filters of size 10"
CN/15/13
Rationalization of product trade names
CN/15/11
Modification/Improvement in product labeling of mdi 25mm Inline Filters and Inline Vent Filters
CN/15/10
Change in Autoclaving temperature specification of mdi Capsule Filters
CN/15/09
Removal of product individual label from mdi Inline Filters and Inline Vent Filters
CN/15/08
Change in Certificate of Quality for mdi Closed Sterility Test Device type Stericheck
CN/15/07
Redefining of product expiry date/shelf life of Gamma Irradiated Products
CN/15/06
Improvement in the identification of mdi products
CN/15/05
Improved design of end connection type 1/4" - 3/8" Hose barb (Code - B) used with mdi Inline Filters and Inline Vent Filter
CN/15/04
New printing on the packaging box for mdi cartridge filters of length 10", 20" and 30" (All types and all pore sizes)
CN/15/03
Improved design of Protective Cap for end connection type Single Step 1/2" Hose barb (Code - Q) used with mdi Capsule Filters
CN/15/02
Modification in identification on mdi Inline Filters and Inline Vent Filters
CN/15/01
Change in product catalog number of Stericheck
CN/14/09
Change in product catalog number of Capsule filter
CN/14/08
Improvement/Modification in identification on Inline Filters and Inline Vent Filters
CN/14/07
Improved/Modified design of mdi Stericheck (Closed Sterility Test System)
CN/14/06
Discontinuation of pack size of mdi Cellulose Nitrate Membrane Disc Filters with Ink Grid
CN/14/05
Addition/change of specification of sterilization for mdi cartridge and capsule filters
CN/14/04
Change in Diffusion Flow Limit for mdi 0.2µm Polyethersulfone membrane Cartridge Filters
CN/14/03
Change in Minimum Bubble Point Test Specification for mdi Nylon membrane Filters
CN/14/02
Assigning Trade Names to the products
CN/14/01
Inclusion of 50% Isopropyl alcohol wetted Bubble Point Test Specification in Certificate of Quality (CoQ) for Nylon Membrane Cartridge Filters (pore sizes: 0.2 3m and 0.45 3m) of length 10".
MB/14/01
Change in Lot numbering system of mdi Pre-sterilized Membrane Disc Filters (All types)
MB/13/04
Change in Certificate of Quality for mdi M-Funnel
CR/13/05
Modification in identification on Cartridge Filter
CP/13/10
Change in Certificate of Quality (CoQ)
CP/13/09
Modification in identification on Capsule Filter of length 2", 5" and 8" (All types)
CP/13/08
Assigning Trade Names to the products
CP/13/07
Separate Identification of Serial number and Sterilization cycle number on Certificate of Quality and product label for filters
CP/13/06
Addition of Cytotoxicity Test to Certificate of Quality for mdi Polyethersulfone membrane Filters
CP/13/05
Improved design of Protective Caps for vent/Drain valve and Inlet/Outlet connection (½" Stepped Hose Barb only) used with mdi Capsule Filters
MB/13/03
Improved/Modified design of Expansion chamber in mdi SVP Diluter (All types)
CR/13/04
Modification in identification on Cartridge Filter (Sizes greater than or equal to 10")
CP/13/01
Change in Bubble Point Test specification for mdi 0.1 µm Polyethersulfone Membrane
Capsule Filter
CR/11/01
Change in Water Intrusion Rate specification for 5" 0.2 µm PTFE Membrane
Cartridge Filters type CPTF and CPTH
CR/13/01
Change in Bubble Point Test specification for mdi 0.1 &m Polyethersulfone
Membrane Cartridge Filter
DP/13/01
Change in Certificate of Quality for mdi RBC Separation Membranes
MB/13/01
Change in Lot numbering system of mdi Funnel (All types)
MB/12/02
Improved packaging (outer carton) for mdi Funnel (All types)
CP/12/02
Modification in identification on 10" Large Capsule Filter (All types)
CP/12/01
Modification in Disc sealing process of 1" Capsule Filter type DKL
MB/12/01
Rationalization of pore size of Membrane Disc Filters type CN/0.22 μm (all diameters)
DP/12/06
Change in Certificate of Quality for mdi Sample Pad Type GFB-R
DP/12/05
Change in Certificate of Quality for mdi Conjugate Release Matrix
DP/12/04
Change in Certificate of Quality for mdi Nitrocellulose Membrane Laminate Type CNPF
DP/12/03
Change in Certificate of Quality for mdi Nitrocellulose Membrane Laminate Type CNPC
DP/12/02
Change in Certificate of Quality for mdi Nitrocellulose Membrane Laminate Type CNPH
DP/12/01
Change in Thickness Specification for RBC Separation Membrane (0.35)
DP/11/02
Change in Certificate of Quality for mdi Conjugate Release Matrix
DP/11/01
Change in Certificate of Quality for mdi Sample Pad type GFB-R
CP/11/01
Rationalization of length of 10" Capsule filter (All capsule types)
MB-11-05
Change in Certificate of Quality for mdi Closed Sterility Test Device type Stericheck (All types)
MB-11-04
Change in mdi Closed Sterility Test Device type Stericheck-SVP1 and Stericheck-SVP3 (All membrane types)
SL/11/01
Change in Printing Matter of mdi Syringe Filters
MB/11/03

Change in mdi Closed Sterility Test Device type Stericheck-SVP2 (All membrane types)

MB/11/02

Change in mdi Closed Sterility Test Device type Stericheck (All types)

MB/11/01

Change in mdi Closed Sterility Test Device Stericheck (All types).

SL/10/02

Outer Ring Color Change of mdi Syringe Filters Type SYTG/0.2 µm (25 mm and 13 mm)

MB/10/04

Change in mdi Closed Sterility Test Device type Stericheck (All Types).

MB/10/03

Change in mdi Closed Sterility Test Device type Stericheck-LVP (All membrane Types).

CP/10/04

New packaging box for mdi capsule filters of length 2”, 5” and 10” (All types and all pore sizes).

CP/10/03
New design of drain valve and vent valve in mdi capsule filters of length 2”, 5” and 10” (All types and all pore sizes).
MB/10/02

Change in mdi Closed Sterility Test Device type Stericheck-C and Stericheck-V (All types).

DP/10/01

Change in Certificate of Quality for mdi Polyester Backed Nitrocellulose Membrane Type CNPH, CNPC and CNPF.

CP/10/02
Change in the specification of autoclave cycles for mdi PTFE membrane capsule filters.
MB/10/01
Change in Grid Printing of mdi Grid Marked Membrane Disc Filters.
SL/10/01
Change in Labelling of mdi Syringe Filters (All types).
CP/09/03
Change in Minimum Bubble Point test specification for mdi Polyethersulfone  membrane products.
MB/09/02

Change in mdi Closed Sterility Test Device Stericheck Type SVP2 (All Membrane Types)

MB/09/03

Change in mdi Closed Sterility Test Device Stericheck (All types).

MB/09/04
Change in mdi Closed Sterility Test Device Stericheck Type PC
(All membrane types).
MB/09/05
Change in mdi Closed Sterility Test Device Stericheck (All types).
MB/09/06
Change in mdi Closed Sterility Test Device Stericheck-C and Stericheck-N
(All types).
MB/09/07
Change in mdi Closed Sterility Test Device Stericheck (All types).
MB/09/08
Change in mdi Closed Sterility Test Device Stericheck-V (All types).
MB/09/09

Change in mdi Closed Sterility Test Device Stericheck (All types).

 
 
 
 
 
 
 
 
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