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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 PRONE AND LATERAL HEAD FRAME WITH SOFT LAYER POLYURETHANE FOAM BLUE DISPOSABLE NOT MADE WITH NATURAL RUBBER LATEX HALYARD FDA UDI
Model / Reference
48716 FDA UDI
Description
FOAM POSITIONER PRONE AND LATERAL HEAD FRAME WITH SOFT LAYER POLYURETHANE FOAM BLUE DISPOSABLE NOT MADE WITH NATURAL RUBBER LATEX HALYARD FDA UDI

Identifiers

Primary DI / UDI-DI
10885632373084 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 deea746e-3796-4409-a5ac-8cd5f2fe8958 33 fields · synced May 30, 2026