Identity
- Trade Name
- Dyna Locking Trochanteric Nail FDA UDI
- Generic Name
- Orthopaedic implant/instrument dismantling device FDA UDI
- Model / Reference
- NG9048 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800015949392 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic implant/instrument dismantling device 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
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic implant/instrument dismantling device
A comprehensive medical device directory, featuring the Dyna Locking Trochanteric Nail orthopaedic manual surgical instrument. This device is designed to dismantle component parts of an implant or surgical instrument, and is typically made from high-grade stainless steel or synthetic material.
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- CG MedTech Co., Ltd.
Sources (1)
- FDA UDI ae7d49e2-d93c-456f-9430-e9e7f9ae7f26 33 fields · synced Jul 17, 2026