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Velofix™ TLIF Cage

FDA UDI

Class I (US FDA UDI)

by CG MedTech Co., Ltd.

Identity

Trade Name
Velofix™ TLIF Cage FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Model / Reference
TL0916 FDA UDI

Identifiers

Primary DI / UDI-DI
08800037575012 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable 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: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
CG MedTech Co., Ltd.

Sources (1)

  • FDA UDI decc8f7d-3eaa-467a-aa6d-93f58653870a 32 fields · synced Jun 8, 2026