← Back to catalogue

Nkx3.1

FDA UDI

Class I (US FDA UDI)

by Biocare Medical, Llc

Identity

Trade Name
NKX3.1 FDA UDI
Generic Name
NKX protein IVD, antibody FDA UDI
Model / Reference
OPAI422T60 FDA UDI

Identifiers

Primary DI / UDI-DI
00847627025111 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
NKX protein IVD, antibody FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Category: NKX protein IVD, antibody

Nkx3.1 by Biocare Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as NKX protein IVD, antibody.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Biocare Medical, Llc

Sources (1)

  • FDA UDI 24b00173-6669-4249-bdd1-1cc1279b86c5 33 fields · synced May 30, 2026