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Dyna Locking Trochanteric Nail™

FDA UDI

Class II (US FDA UDI)

by CG MedTech Co., Ltd.

Identity

Trade Name
Dyna Locking Trochanteric Nail™ FDA UDI
Generic Name
Femur intramedullary nail FDA UDI
Model / Reference
NG111134R FDA UDI

Identifiers

Primary DI / UDI-DI
08800015939508 FDA UDI
510(k) Number
K093707 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Femur intramedullary nail FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

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: Femur intramedullary nail

Dyna Locking Trochanteric Nail™ by CG MedTech Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femur intramedullary nail.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI af52c9df-4715-4002-9052-17bb2ae38af7 34 fields · synced May 30, 2026