← Back to catalogue

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
HALYARD* LOWER EXTREMITY Drape FDA UDI
Model / Reference
13232 FDA UDI
Description
HALYARD* LOWER EXTREMITY Drape FDA UDI

Identifiers

Catalog Number
13232NS FDA UDI
Primary DI / UDI-DI
10680651132328 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

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

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
O&M Halyard, Inc.

Sources (1)

  • FDA UDI cd036d27-d599-411d-95b6-f4cbd30bc938 35 fields · synced Jun 8, 2026