← Back to catalogue

Em

FDA UDI

Class I (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
EM FDA UDI
Generic Name
Cervical spine collar, reusable FDA UDI
Device Name
COLLAR CINCH FDA UDI
Model / Reference
L593 FDA UDI
Description
COLLAR CINCH FDA UDI

Identifiers

Primary DI / UDI-DI
00026072022276 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Cervical spine collar, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Cervical spine collar, reusable

Em by Allied Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical spine collar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI 4082ec49-9d75-4a0f-8078-cd666431483e 33 fields · synced May 30, 2026