Biolog, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Biolog, Inc. makes
Biolog, Inc. manufactures transport systems for biological samples, including the GC TRANSPORT SYSTEM and JEMBEC TRANSPORT SYSTEM, as well as culture media for microbiological testing, such as the GC CULTURE MEDIUM and SELECTIVE GC CULTURE MEDIUM. The company also produces disposable ostomy pouches, including a DISPOSABLE UROSTOMY POUCH and a DRAINABLE POUCH for ileostomy and colostomy applications.
The company’s products are regulated under FDA’s Class I and Class II device classifications, with relevant submissions listed in the FDA’s 510(k) registry. These devices are intended for use in the United States, where the manufacturer is based.
Catalogue
Gc Ttansport System Ref K811284
Regimes: 510(k) Registry: 510(k)Gc Culture Medium Ref K811281
Regimes: 510(k) Registry: 510(k)Selective Gc Culture Medium Ref K811282
Regimes: 510(k) Registry: 510(k)Jembec Transport System Ref K811283
Regimes: 510(k) Registry: 510(k)Disposable Urostomy Pouch Ref K850750
Regimes: 510(k) Registry: 510(k)Dispos. Drainabel Pouch For Ileostomy/Colostomy Ref K850751
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biolog, Inc. have in the registry?
The registry currently lists 6 devices for Biolog, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biolog, Inc.'s devices?
Among its 6 most recently registered devices, Biolog, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Biolog, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Biolog, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biolog, Inc. in the registry?
The most recently registered devices listed for Biolog, Inc. include GC TTANSPORT SYSTEM, GC CULTURE MEDIUM, SELECTIVE GC CULTURE MEDIUM and JEMBEC TRANSPORT SYSTEM.