← Back to catalogue

Harness Cervical Visual

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
HARNESS CERVICAL VISUAL FDA UDI
Generic Name
Horizontal non-powered traction system FDA UDI
Model / Reference
920877 FDA UDI

Identifiers

Catalog Number
2970011818 FDA UDI
Primary DI / UDI-DI
00733657237672 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Horizontal non-powered traction system 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Horizontal non-powered traction system

Harness Cervical Visual by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Horizontal non-powered traction system.

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
AliMed, LLC

Sources (1)

  • FDA UDI 3d3d704b-78a1-4285-9cff-dc7e822d1ac9 34 fields · synced Jun 9, 2026