← Back to catalogue

Velofix™ SA Cervical Cage

FDA UDI

Class I (US FDA UDI)

by CG MedTech Co., Ltd.

Identity

Trade Name
Velofix™ SA Cervical Cage FDA UDI
Generic Name
Orthopaedic implant/instrument assembling device FDA UDI
Model / Reference
TSS1014 FDA UDI

Identifiers

Primary DI / UDI-DI
08800037567505 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Orthopaedic implant/instrument assembling device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant/instrument assembling device

Velofix™ SA Cervical Cage by CG MedTech Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant/instrument assembling device.

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

Sources (1)

  • FDA UDI 54b6fdb3-ed89-48f2-87fd-0645466f9ebd 32 fields · synced Jun 6, 2026