Identity
- Trade Name
- 2.0 Cannulated Drill FDA UDI
- Generic Name
- Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile FDA UDI
- Device Name
- 2.0mm Cannulated Drill, 165mm FDA UDI
- Model / Reference
- MDS101120165C FDA UDI
- Description
- 2.0mm Cannulated Drill, 165mm FDA UDI
Identifiers
- Catalog Number
- MDS101120165C FDA UDI
- Primary DI / UDI-DI
- 10812269022801 FDA UDI
- FDA Product Code
- HWC FDA UDIHRS FDA UDI
- GMDN Term
- Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3040 FDA UDI888.3030 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 165 Millimeter FDA UDIOuter Diameter — 2.0 Millimeter FDA UDI
Category: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterileCannulated surgical drill bit, single-use, non-sterile
2.0 Cannulated Drill by Miami Device Solutions — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cannulated surgical drill bit, single-use, non-sterile.
- FO NX Nail System — FIELD ORTHOPAEDICS PTY LTD · Class I
- TopLock — FUSION ORTHOPEDICS, LLC · Class II
- HammerTech — FUSION ORTHOPEDICS, LLC · Class II
- TopLock — FUSION ORTHOPEDICS, LLC · Class II
- FO NX Nail System — FIELD ORTHOPAEDICS PTY LTD · Class I
- LapiLock — FUSION ORTHOPEDICS, LLC · Class II
- FuzeFix Large — FUSION ORTHOPEDICS, LLC · Class II
- PolyLock — FUSION ORTHOPEDICS, LLC · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Miami Device Solutions
Sources (1)
- FDA UDI f0ac16ac-49ba-44aa-9620-42225cb971e4 36 fields · synced May 30, 2026