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Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Surgical instrument interim-placement holder, reusable FDA UDI
Device Name
Instrument Cassette 16 SS FDA UDI
Model / Reference
1124965 FDA UDI
Description
Instrument Cassette 16 SS FDA UDI

Identifiers

Catalog Number
1124965 FDA UDI
Primary DI / UDI-DI
H65811249651 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Surgical instrument interim-placement holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical instrument interim-placement holder, reusable

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

Similar devices

Also classified as Surgical instrument interim-placement holder, reusable.

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 c016748e-9a6a-458b-9a5d-c440fe1cfcbf 34 fields · synced Jun 1, 2026