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BioMaxima Spółka Akcyjna devices, product family

by BioMaxima Spółka Akcyjna 10 variants Basic UDI-DI 59026439ASCRSAP7

Shared by every variant

Manufacturer
BioMaxima Spółka Akcyjna(10)
Basic UDI-DI
59026439ASCRSAP7
Risk class
Class A
Legislation
IVDR
Market status
10 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 59026439ASCRSAP7.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 10 devices listed on this page; other pages of the family can carry others.

Variants

10 devices · page 1 of 1

Variants of BioMaxima Spółka Akcyjna devices, Basic UDI-DI 59026439ASCRSAP7
UDI-DISize and differences
Chromagar™ Salmonella PLUS PP 002805902643929319
Sterilised before use: no
On the market
Chromagar™ Salmonella Plus LAB-AGAR™ BT 5275.0505902643951181
Sterilised before use: no
On the market
Chromogenic Salmonella LAB-AGAR™ BT 5072.0105902643946095
Sterilised before use: no
On the market
Chromogenic Salmonella LAB-AGAR™ BT 5072.0205902643946101
Sterilised before use: no
On the market
Chromogenic Salmonella LAB-AGAR™ BT 5072.0505902643950238
Sterilised before use: no
On the market
Chromogenic Salmonella LAB-AGAR™ PP 011505902643929326
Sterilised before use: no
On the market
Chromogenic Salmonella LAB-AGAR™ PS 598- 10005902643914858
Sterilised before use: yes
On the market
Chromogenic Salmonella LAB-AGAR™ PS 598- 25005902643985353
Sterilised before use: yes
On the market
Chromogenic Salmonella LAB-AGAR™ PS 598- 50005902643904859
Sterilised before use: no
On the market
Chromogenic Salmonella LAB-AGAR™ PS 598A- 50005902643906129
Sterilised before use: no
On the market