Identity
- Trade Name
- MULTILOC FDA UDI
- Generic Name
- Orthopaedic x-ray ruler FDA UDI
- Device Name
- RADIOGRAPHIC RULER FOR MULTILOC HUMERAL NAIL FDA UDI
- Model / Reference
- 03.019.001 FDA UDI
- Description
- RADIOGRAPHIC RULER FOR MULTILOC HUMERAL NAIL FDA UDI
Identifiers
- Catalog Number
- 03019001 FDA UDI
- Primary DI / UDI-DI
- 10886982069368 FDA UDI
- 510(k) Number
- K120807 FDA UDI
- FDA Product Code
- HSB FDA UDI
- GMDN Term
- Orthopaedic x-ray ruler 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
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
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
Category: Orthopaedic x-ray ruler
Multiloc by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic x-ray ruler.
- Radiographic Ruler — Double Medical Technology Inc. · Class II
- Piccolo Composite Nailing System — CARBOFIX ORTHOPEDICS LTD · Class II
- PRECICE® Instruments — NuVasive Specialized Orthopedics, Inc. · Class I
- RADIOGRAPHIC RULER, ANTEGRADE/RETROGRADE — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class I
- Response Rib and Pelvic System — ORTHOPEDIATRICS CORP. · Class I
- COOLIEF* SINERGY* Epsilon* Ruler — Avanos Medical, Inc. · Class I
- X-Ray Ruler — I.T.S. GmbH · Class I
- PRECICE® Intramedullary Limb Lengthening System Instrument — NuVasive Specialized Orthopedics, Inc. · Class I
Cleared under the same submission
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
- Synthes
Sources (1)
- FDA UDI b5e8a139-5ec6-4e12-891a-151571341cc8 36 fields · synced Jun 8, 2026