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Halyard

FDA UDI

Class II (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
HALYARD FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Equipment Cover Band Bags Clear Polyurethane 12IN x 18IN Polyurethane Clear Non-Sterile CA/100 Not made with Natural Rubber Latex HALYARD FDA UDI
Model / Reference
55886 FDA UDI
Description
Equipment Cover Band Bags Clear Polyurethane 12IN x 18IN Polyurethane Clear Non-Sterile CA/100 Not made with Natural Rubber Latex HALYARD FDA UDI

Identifiers

Primary DI / UDI-DI
20885632425469 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use 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

Yes

FDA UDI

Category: Medical equipment/instrument drape, single-use

Halyard by Owens & Minor Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4b47574f-03e5-4b65-99ec-f55264f13077 33 fields · synced May 30, 2026