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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
Medical equipment drape, single-use, non-sterile FDA UDI
Device Name
X Ray COVER 15x26 FDA UDI
Model / Reference
5701319 FDA UDI
Description
X Ray COVER 15x26 FDA UDI

Identifiers

Catalog Number
5701319 FDA UDI
Primary DI / UDI-DI
10304040103910 FDA UDI
FDA Product Code
NRU FDA UDI
GMDN Term
Medical equipment drape, single-use, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6250 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

No

FDA UDI

Over-the-Counter

Yes

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: Medical equipment drape, single-use, non-sterile

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

Similar devices

Also classified as Medical equipment drape, single-use, non-sterile.

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 11d0079d-2281-4b37-9572-53e156fe54fe 34 fields · synced Jun 7, 2026