← Back to catalogue

Fb

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 70562

by Biomerieux , Inc.

Identity

Trade Name
FB EUDAMEDFDA UDI
Generic Name
Multiple Staphylococcus bacterial species culture isolate identification IVD, kit FDA UDI
Device Name
FB EUDAMED
FB is a reagent associated to API® Campy (20 800), ID 32 STAPH (32 500), rapid ID 32 A (32 300), rapid ID 32 STREP (32 600) FDA UDI
Model / Reference
70562 EUDAMEDFDA UDI
Description
FB is a reagent associated to API® Campy (20 800), ID 32 STAPH (32 500), rapid ID 32 A (32 300), rapid ID 32 STREP (32 600) FDA UDI

Identifiers

Primary DI / UDI-DI
03573026099923 EUDAMEDFDA UDI
Basic UDI-DI
357302BUDI000284TL EUDAMED
FDA Product Code
JTO FDA UDI
EMDN Code
W0104080299 MANUAL IDENTIFICATION - OTHER EUDAMED
GMDN Term
Multiple Staphylococcus bacterial species culture isolate identification IVD, kit FDA UDI

Classification

Device Class
Class B EUDAMED
Class I FDA UDI
Regulation Number
866.2660 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple Staphylococcus bacterial species culture isolate identification IVD, kit

Fb by Biomerieux , Inc. — Class I — IVDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Multiple Staphylococcus bacterial species culture isolate identification IVD, kit.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

IVDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biomerieux , Inc.

Sources (2)

  • FDA UDI 05ca5eb8-161e-49ca-a5d2-884bfa4bb852 34 fields · synced Jun 11, 2026
  • EUDAMED 019dbea2-7daf-49e8-87f2-589bb3aab33a 61 fields · synced Jun 11, 2026