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HemosIL RecombiPlasTin 2G (8 mL)

FDA UDI

Class II (US FDA UDI)

by Instrumentation Laboratory Company

Identity

Trade Name
HemosIL RecombiPlasTin 2G (8 mL) FDA UDI
Generic Name
Prothrombin time (PT) IVD, kit, clotting FDA UDI
Device Name
HemosIL RecombiPlasTin 2G (8 mL) FDA UDI
Model / Reference
00020002950 FDA UDI
Description
HemosIL RecombiPlasTin 2G (8 mL) FDA UDI

Identifiers

Catalog Number
00020002950 FDA UDI
Primary DI / UDI-DI
08426950453079 FDA UDI
FDA Product Code
GJS FDA UDI
GMDN Term
Prothrombin time (PT) IVD, kit, clotting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7750 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Prothrombin time (PT) IVD, kit, clotting

HemosIL RecombiPlasTin 2G (8 mL) by Instrumentation Laboratory Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Prothrombin time (PT) IVD, kit, clotting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 320339f8-6bf3-4e30-8765-981971f60794 36 fields · synced May 31, 2026