Identity
- Trade Name
- CORE FDA UDI
- Generic Name
- Drilling power tool attachment, basic FDA UDI
- Device Name
- Aria Dura Guard Attachment FDA UDI
- Model / Reference
- 5400210158 FDA UDI
- Description
- Aria Dura Guard Attachment FDA UDI
Identifiers
- Catalog Number
- 5400-210-158 FDA UDI
- Primary DI / UDI-DI
- 07613154500062 FDA UDI
- FDA Product Code
- HBB FDA UDI
- GMDN Term
- Drilling power tool attachment, basic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4370 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
MR Conditional FDA UDI
Category: Drilling power tool attachment, basic
Core by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Drilling power tool attachment, basic.
- Smith and Nephew — Provision · Class I
- Stryker — Provision · Class I
- Treace Medical Concepts — Provision · Class I
- Synthes — Provision · Class I
- Treace Medical Concepts — Provision · Class I
- GEO — Provision · Class I
- Synthes — Provision · Class I
- CrossRoads — Provision · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI 22b5e5d1-14f1-4085-99db-d1bd7e9ca14f 36 fields · synced Jun 1, 2026