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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
Skin stapler FDA UDI
Device Name
Stapler Skin Disposable 35R FDA UDI
Model / Reference
9009734 FDA UDI
Description
Stapler Skin Disposable 35R FDA UDI

Identifiers

Catalog Number
9009734 FDA UDI
Primary DI / UDI-DI
00304040029091 FDA UDI
FDA Product Code
GAG FDA UDI
GMDN Term
Skin stapler FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 5.9 Millimeter FDA UDI

Category: Skin stapler

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

Similar devices

Also classified as Skin stapler.

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 66c39b07-bf48-4d80-851e-2303966c4843 36 fields · synced Jun 6, 2026