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Halyard

FDA UDI

Class I (US FDA UDI)

by Owens & Minor Distribution, Inc.

Identity

Trade Name
Halyard FDA UDI
Generic Name
Freestanding headrest, single-use FDA UDI
Device Name
FOAM POSITIONER SUPINE HEAD DONUT MULTI RING POLYURETHANE FOAM BLUE DISPOSABLE NOT MADE WITH NATURAL RUBBER LATEX HALYARD FDA UDI
Model / Reference
48722 FDA UDI
Description
FOAM POSITIONER SUPINE HEAD DONUT MULTI RING POLYURETHANE FOAM BLUE DISPOSABLE NOT MADE WITH NATURAL RUBBER LATEX HALYARD FDA UDI

Identifiers

Primary DI / UDI-DI
10885632373145 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Freestanding headrest, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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: Freestanding headrest, single-use

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

Similar devices

Also classified as Freestanding headrest, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 10012f24-9726-4e86-a84d-82b7f3d38e0f 33 fields · synced May 30, 2026