Identity
- Trade Name
- Comprehensive Shoulder System FDA UDI
- Generic Name
- Coated shoulder humeral stem prosthesis FDA UDI
- Model / Reference
- 12-113564 FDA UDI
Identifiers
- Catalog Number
- 12-113564 FDA UDI
- Primary DI / UDI-DI
- 00880304591578 FDA UDI
- FDA Product Code
- KWT FDA UDIHSD FDA UDIKWS FDA UDIMBF FDA UDIPHX FDA UDI
- GMDN Term
- Coated shoulder humeral stem prosthesis FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3650 FDA UDI888.3690 FDA UDI888.3660 FDA UDI888.3670 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Coated shoulder humeral stem prosthesis
Comprehensive Shoulder System by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Coated shoulder humeral stem prosthesis.
- OsseoFit™ Stemless Shoulder — Zimmer, Inc. · Class II
- TORNIER PERFORM™ HUMERAL SYSTEM — TORNIER, INC. · Class II
- Tornier HRS — TORNIER, INC. · Class II
- Trabecular Metal® — Zimmer, Inc. · Class II
- INHANCE — DEPUY (IRELAND) · Class II
- Aequalis™ PerFORM+ — TORNIER, INC. · Class II
- Trabecular Metal® — Zimmer, Inc. · Class II
- Tornier Perform® Anatomic Augmented Glenoid — TORNIER, INC. · Class II
Cleared under the same submission
K140652 also covers:
- BIO-MODULAR — Biomet Orthopedics, Inc.
- BIO-MODULAR — Biomet Orthopedics, Inc.
- BIO-MODULAR — Biomet Orthopedics, Inc.
- BIO-MODULAR — Biomet Orthopedics, Inc.
- BIO-MODULAR — Biomet Orthopedics, Inc.
- BIO-MODULAR — Biomet Orthopedics, Inc.
- Comprehensive Shoulder System — Biomet Orthopedics, Inc.
- Comprehensive Shoulder System — Biomet Orthopedics, Inc.
- Comprehensive Shoulder System — Biomet Orthopedics, Inc.
- Comprehensive Shoulder System — Biomet Orthopedics, Inc.
- Comprehensive Shoulder System — Biomet Orthopedics, Inc.
K193038 also covers:
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE SHOULDER SYSTEM — Biomet Orthopedics, Inc.
- COMPREHENSIVE(R) SHOULDER 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 Orthopedics, Inc.
Sources (1)
- FDA UDI 8e24071a-b99d-4707-98b0-dbaeead472b2 36 fields · synced Jun 1, 2026