Change Notice
 
 
Change Notice No.
Description
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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-11-05
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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