← Back to catalogue

Blood Agar Base No 2

EUDAMEDFDA UDI

Class A (EU MDR)

Ref CM0271TRef CM0055TRef CM0271KRef CM0271BRef CM0271R

by Oxoid Ltd

Identity

Trade Name
BLOOD AGAR BASE NO 2 EUDAMEDFDA UDI
BLOOD AGAR BASE EUDAMED
Generic Name
Basic/simple nutrient agar culture medium IVD FDA UDI
Device Name
BLOOD AGAR BASE NO 2 EUDAMED
BLOOD AGAR BASE EUDAMED
Model / Reference
CM0271T EUDAMED
CM0055T EUDAMED
CM0271K EUDAMED
CM0271B EUDAMEDFDA UDI
CM0271R EUDAMED

Identifiers

Primary DI / UDI-DI
05032384002245 EUDAMED
05032384001323 EUDAMED
05032384002221 EUDAMED
05032384002214 EUDAMEDFDA UDI
05032384002238 EUDAMED
Basic UDI-DI
5032384BloodAgrBase2BD EUDAMED
5032384BloodAgrBaseMW EUDAMED
FDA Product Code
JSG FDA UDI
EMDN Code
W0104010101 DEHYDRATED CULTURE MEDIA (DCM) EUDAMED
GMDN Term
Basic/simple nutrient agar culture medium IVD FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
866.2300 FDA UDI
Market of Registration
Netherlands 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

Yes

EUDAMED

Microbial Substances

Yes

EUDAMEDEUDAMED

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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

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

Blood Agar Base No 2 by Oxoid Ltd — Class A — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Oxoid Ltd
EUDAMED SRN
GB-MF-000016914
Authorised Representative
Thermo Fisher Diagnostics B.V. NL-AR-000013157

Sources (6)

  • EUDAMED bd75871c-b97c-47c5-a49e-7e9a05227867 61 fields · synced Aug 1, 2026
  • EUDAMED 11f44848-31f7-4926-a37a-fdc94adca7e7 61 fields · synced May 17, 2026
  • EUDAMED 1e8b73c0-88eb-4aef-bfac-1188ccd992c8 61 fields · synced May 17, 2026
  • EUDAMED 838febeb-2e3e-4370-bc57-269f239e4eac 61 fields · synced May 18, 2026
  • FDA UDI 20570b97-2759-46b7-87bd-cf018973abeb 32 fields · synced May 30, 2026
  • EUDAMED c8246177-49fb-4f8f-9cea-1425642fd539 61 fields · synced Jul 12, 2026