Identity
- Trade Name
- A.L.P.S.CORTICAL TAP FDA UDI
- Generic Name
- Bone tap, single-use FDA UDI
- Model / Reference
- 8241-50-170 FDA UDI
Identifiers
- Catalog Number
- 824150170 FDA UDI
- Primary DI / UDI-DI
- 00887868049057 FDA UDI
- FDA Product Code
- HWX FDA UDI
- GMDN Term
- Bone tap, single-use 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
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Bone tap, single-use
A.l.p.s.cortical Tap by Biomet Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bone tap, single-use.
- EVOS — Smith & Nephew, Inc. · Class II
- Spine Instruments — Medacta International · Class I
- CODA™ Anterior Cervical Plate System — Pioneer Surgical Technology, Inc. · Class I
- Flower Orthopedics — FLOWER ORTHOPEDICS CORPORATION · Class I
- DELTA — Stryker Leibinger · Class II
- DELTA — Stryker Leibinger · Class II
- Nobel Biocare® — Nobel Biocare AG · Class I
- Asnis — Stryker Corp. · 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
- Biomet Orthopedics, Inc.
Sources (1)
- FDA UDI 3acb9c92-7289-45f7-94e8-b5acf7a08d3c 35 fields · synced May 30, 2026