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Cardboard Head Immobilizer

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Cardboard Head Immobilizer FDA UDI
Generic Name
Head/neck immobilizer, single-use FDA UDI
Device Name
Cardboard Head Immobilizer FDA UDI
Model / Reference
5627 FDA UDI
Description
Cardboard Head Immobilizer FDA UDI

Identifiers

Primary DI / UDI-DI
00616784562735 FDA UDI
FDA Product Code
MRI FDA UDI
GMDN Term
Head/neck immobilizer, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3490 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Head/neck immobilizer, single-use

Cardboard Head Immobilizer by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Head/neck immobilizer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI acd4e38b-9f63-43cb-9e0c-ed3ff94bf91b 33 fields · synced Jun 8, 2026