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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
Bandage scissors, reusable FDA UDI
Device Name
Scissors Utility & Bandage FDA UDI
Model / Reference
1049280 FDA UDI
Description
Scissors Utility & Bandage FDA UDI

Identifiers

Catalog Number
1049280 FDA UDI
Primary DI / UDI-DI
00304040022696 FDA UDI
FDA Product Code
LGG FDA UDI
GMDN Term
Bandage scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5980 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bandage scissors, reusable

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

Similar devices

Also classified as Bandage scissors, 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 53923922-aa36-4e4f-b8fc-df0e4cd654cb 34 fields · synced Jun 6, 2026