Identity
- Trade Name
- VELYS FDA UDI
- Generic Name
- Stereotactic surgery system probe, single-use FDA UDI
- Device Name
- VELYS Robotic-Assisted Solution ARRAY SET - KNEE FDA UDI
- Model / Reference
- 4515-70-001 FDA UDI
- Description
- VELYS Robotic-Assisted Solution ARRAY SET - KNEE FDA UDI
Identifiers
- Catalog Number
- 451570001 FDA UDI
- Primary DI / UDI-DI
- 10603295519072 FDA UDI
- FDA Product Code
- OLO FDA UDI
- GMDN Term
- Stereotactic surgery system probe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 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
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: Stereotactic surgery system probe, single-use
Velys by Depuy (ireland) — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Depuy (ireland)
Sources (1)
- FDA UDI c592054f-b962-4123-b91b-0b1407755a03 35 fields · synced Jun 6, 2026