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Status iFOBTest Collection Tube Kit

FDA UDI

by Princeton Biomeditech Corp.

Identity

Trade Name
Status iFOBTest Collection Tube Kit FDA UDI
Generic Name
Faecal occult blood IVD, reagent FDA UDI
Device Name
Status iFOBTest Collection Tube Kit (50Tubes) FDA UDI
Model / Reference
BSP-300-TU-01 FDA UDI
Description
Status iFOBTest Collection Tube Kit (50Tubes) FDA UDI

Identifiers

Catalog Number
BSP-300-TU-01 FDA UDI
Primary DI / UDI-DI
10743816001096 FDA UDI
GMDN Term
Faecal occult blood IVD, reagent FDA UDI

Classification

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

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

Category: Faecal occult blood IVD, reagent

Status iFOBTest Collection Tube Kit by Princeton Biomeditech Corp. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Faecal occult blood IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Princeton Biomeditech Corp.

Sources (1)

  • FDA UDI 58099d8a-eebc-4d20-be32-e02a28a7c590 36 fields · synced May 30, 2026