← Back to catalogue

Bacticard Neisseria

EUDAMEDFDA UDI

Class A (EU MDR)

Ref R21110

by Remel, Inc.

Identity

Trade Name
BACTICARD NEISSERIA EUDAMED
BACTICARD FDA UDI
Generic Name
Neisseria gonorrhoeae culture isolate antigen IVD, kit, agglutination FDA UDI
Device Name
BACTICARD NEISSERIA EUDAMED
BactiCard Neisseria 25TST/KT FDA UDI
Model / Reference
R21110 EUDAMEDFDA UDI
Description
BactiCard Neisseria 25TST/KT FDA UDI

Identifiers

Catalog Number
R21110 FDA UDI
Primary DI / UDI-DI
00848838022470 EUDAMEDFDA UDI
Basic UDI-DI
8488380BctCrdNeisseriaBV EUDAMED
FDA Product Code
JSX FDA UDI
EMDN Code
W0104080201 GRAM NEGATIVE - MANUAL IDENTIFICATION EUDAMED
GMDN Term
Neisseria gonorrhoeae culture isolate antigen IVD, kit, agglutination FDA UDI

Classification

Device Class
Class A EUDAMED
Class I FDA UDI
Regulation Number
866.2660 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

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

No

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

Bacticard Neisseria by Remel, Inc. — 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
Remel, Inc.
EUDAMED SRN
US-MF-000044686
Authorised Representative
Thermo Fisher Diagnostics B.V. NL-AR-000013157

Sources (2)

  • EUDAMED a8cd3edf-0910-410b-9d1e-5241b02dd98f 61 fields · synced Jul 10, 2026
  • FDA UDI 5997f21d-8b01-477b-9ed1-587f23493066 34 fields · synced May 30, 2026