Cervmax®

FDA UDI

Class I (US FDA UDI)

by Pmt Corp.

Identity

Trade Name: CERVMAX® FDA UDI
Generic Name: Cervical spine collar, single-use FDA UDI
Device Name: CERVMAX CTO BRACE, ANTERIOR SUPPORT, ADULT/1565 SHORT FDA UDI
Model / Reference: 1625-6AB FDA UDI
Description: CERVMAX CTO BRACE, ANTERIOR SUPPORT, ADULT/1565 SHORT FDA UDI

Identifiers

Primary DI / UDI-DI: 00650551146087 FDA UDI
FDA Product Code: IQK FDA UDI
GMDN Term: Cervical spine collar, 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cervical spine collar, single-use

Cervmax® by Pmt Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Cervical spine collar, single-use.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Pmt Corp.

Sources (1)

FDA UDI f602b688-2f95-484f-96bb-dbf3afa7275a 33 fields · synced Jun 8, 2026