← Back to catalogue

Hemosure®

FDA UDI

Class II (US FDA UDI)

by Hemosure Inc.

Identity

Trade Name
HEMOSURE® FDA UDI
Generic Name
Faecal occult blood IVD, kit, rapid ICT, clinical FDA UDI
Device Name
Hemosure FOB Buffer Tube Plain Box Set (100 Purple Cap Tubes with Long Labels) FDA UDI
Model / Reference
T1-TB100L FDA UDI
Description
Hemosure FOB Buffer Tube Plain Box Set (100 Purple Cap Tubes with Long Labels) FDA UDI

Identifiers

Catalog Number
T1-TB100L FDA UDI
Primary DI / UDI-DI
00817763021841 FDA UDI
FDA Product Code
KHE FDA UDI
GMDN Term
Faecal occult blood IVD, kit, rapid ICT, clinical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Faecal occult blood IVD, kit, rapid ICT, clinical

Hemosure® by Hemosure Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Faecal occult blood IVD, kit, rapid ICT, clinical.

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
Hemosure Inc.

Sources (1)

  • FDA UDI a0b7a810-d965-48b8-b094-30efe8cf55a0 34 fields · synced May 30, 2026