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Halyard

FDA UDI

Class II (US FDA UDI)

by O&M Halyard, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Patient surgical drape, single-use, non-sterile FDA UDI
Device Name
HYH,LRG,DRAPE,-,76X55,36 FDA UDI
Model / Reference
47622 FDA UDI
Description
HYH,LRG,DRAPE,-,76X55,36 FDA UDI

Identifiers

Catalog Number
47622 FDA UDI
Primary DI / UDI-DI
10680651476224 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Patient surgical drape, single-use, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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: Patient surgical drape, single-use, non-sterile

Halyard by O&M Halyard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient surgical drape, single-use, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
O&M Halyard, Inc.

Sources (1)

  • FDA UDI cff0b058-cd67-4bd9-b0c0-f0ecc5df8f85 35 fields · synced May 31, 2026