Identity
- Trade Name
- Arcos® Revision Hip Instrumentation FDA UDI
- Generic Name
- Orthopaedic trocar blade, reusable FDA UDI
- Model / Reference
- 31-301919 FDA UDI
Identifiers
- Catalog Number
- 31-301919 FDA UDI
- Primary DI / UDI-DI
- 05019279431533 FDA UDI
- 510(k) Number
- K100469 FDA UDI
- FDA Product Code
- JDI FDA UDIMAY FDA UDILPH FDA UDIKWZ FDA UDIKWY FDA UDIMEH FDA UDILZO FDA UDI
- GMDN Term
- Orthopaedic trocar blade, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3350 FDA UDI888.3353 FDA UDI888.3358 FDA UDI888.3310 FDA UDI888.3390 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic trocar blade, reusable
Arcos® Revision Hip Instrumentation by Biomet Uk Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic trocar blade, reusable.
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Cleared under the same submission
K100469 also covers:
- ARCOS — Biomet Orthopedics, Inc.
- ARCOS — Biomet Orthopedics, Inc.
- ARCOS — Biomet Orthopedics, Inc.
- ARCOS — Biomet Orthopedics, Inc.
- ARCOS — Biomet Orthopedics, Inc.
- ARCOS — Biomet Orthopedics, Inc.
- ARCOS MODULAR REVISION SYSTEM — Biomet Orthopedics, Inc.
- ARCOS MODULAR REVISION SYSTEM — Biomet Orthopedics, Inc.
- ARCOS MODULAR REVISION SYSTEM — Biomet Orthopedics, Inc.
- ARCOS MODULAR REVISION SYSTEM — Biomet Orthopedics, Inc.
- ARCOS MODULAR REVISION SYSTEM — Biomet Orthopedics, Inc.
- ARCOS MODULAR REVISION SYSTEM — Biomet Orthopedics, Inc.
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 |
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Manufacturer
- Manufacturer
- Biomet Uk Ltd
Sources (1)
- FDA UDI 8e4e3c94-49c0-4586-862c-75db9f8bb90d 35 fields · synced Jun 8, 2026