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4+ Streptavidin AP Label

FDA UDI

Class I (US FDA UDI)

by Biocare Medical, Llc

Identity

Trade Name
4+ Streptavidin AP Label FDA UDI
Generic Name
Streptavidin-enzyme conjugate reagent IVD FDA UDI
Device Name
Alternate name : 4plus Streptavidin AP Label FDA UDI
Model / Reference
AP605H FDA UDI
Description
Alternate name : 4plus Streptavidin AP Label FDA UDI

Identifiers

Primary DI / UDI-DI
00847627003829 FDA UDI
FDA Product Code
NJT FDA UDI
GMDN Term
Streptavidin-enzyme conjugate reagent IVD 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: Streptavidin-enzyme conjugate reagent IVD

4+ Streptavidin AP Label by Biocare Medical, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Streptavidin-enzyme conjugate reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 94bc7822-7cfe-4110-b1c9-3309601f4ffa 34 fields · synced May 30, 2026