Identity
- Trade Name
- arcad® FDA UDI
- Generic Name
- Orthopaedic intraoperative positioning pin, reusable FDA UDI
- Device Name
- Positionning pin Ø3 FDA UDI
- Model / Reference
- XPP01002 FDA UDI
- Description
- Positionning pin Ø3 FDA UDI
Identifiers
- Catalog Number
- XPP01002 FDA UDI
- Primary DI / UDI-DI
- 03700879500973 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic intraoperative positioning pin, reusable 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic intraoperative positioning pin, reusable
arcad® by Novastep — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic intraoperative positioning pin, reusable.
- Omnia Medical Coupler-C — Omnia Medical · Class II
- TriLeap Lower Extremity Anatomic Plating System — CROSSROADS EXTREMITY SYSTEMS LLC · Class I
- UniSyn Hip System — SHALBY ADVANCED TECHNOLOGIES, INC. · Class I
- TrabecuLink Femoral and Tibial Cone - Instruments — WALDEMAR LINK GmbH & Co. KG · Class I
- SPARK - Instruments — WALDEMAR LINK GmbH & Co. KG · Class I
- TriLeap Lower Extremity Anatomic Plating System — CROSSROADS EXTREMITY SYSTEMS LLC · Class I
- Summa Orthopaedics System Surgical Instrument — Jeil Medical Corporation · Class I
- Holding Pin — UNIQUE SURGICAL, LLC · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Novastep
Sources (1)
- FDA UDI a548388f-d467-463d-8b1b-1ec26bd1e986 35 fields · synced May 31, 2026