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Dyna Locking IM Nail

FDA UDI

Class I (US FDA UDI)

by CG MedTech Co., Ltd.

Identity

Trade Name
Dyna Locking IM Nail FDA UDI
Generic Name
Medullary canal orthopaedic reamer, flexible FDA UDI
Model / Reference
IN1037 FDA UDI

Identifiers

Primary DI / UDI-DI
08800015956857 FDA UDI
FDA Product Code
HTO FDA UDI
GMDN Term
Medullary canal orthopaedic reamer, flexible FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Medullary canal orthopaedic reamer, flexible

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

Similar devices

Also classified as Medullary canal orthopaedic reamer, flexible.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d22a494-cc3d-4593-939f-f89aec0084f8 33 fields · synced Jun 8, 2026