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Henry Schein

FDA UDI

Class II (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Faecal specimen collection kit IVD, home-use FDA UDI
Device Name
One Step iFOBT Return Mailers FDA UDI
Model / Reference
9004416 FDA UDI
Description
One Step iFOBT Return Mailers FDA UDI

Identifiers

Catalog Number
9004416 FDA UDI
Primary DI / UDI-DI
00304040002568 FDA UDI
FDA Product Code
KHE FDA UDI
GMDN Term
Faecal specimen collection kit IVD, home-use 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Faecal specimen collection kit IVD, home-use

Henry Schein by Henry Schein, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Faecal specimen collection kit IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Henry Schein, Inc.

Sources (1)

  • FDA UDI 02667ef8-21c2-4a04-b783-a04b2d6e98bd 36 fields · synced May 30, 2026