Identity
- Trade Name
- Invivo FDA UDI
- Generic Name
- Stereotactic system application software FDA UDI
- Device Name
- UroNAV Fusion Biopsy System FDA UDI
- Model / Reference
- 784012 FDA UDI
- Description
- UroNAV Fusion Biopsy System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884838081543 FDA UDI
- 510(k) Number
- K053610 FDA UDI
- FDA Product Code
- JAK FDA UDI
- GMDN Term
- Stereotactic system application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1750 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
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Stereotactic system application software
Invivo by Philips DS North America LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K053610 also covers:
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
- Philips DS North America LLC
Sources (1)
- FDA UDI e7cc8a5b-c2d2-4ce4-a01f-9c1f489c9d84 36 fields · synced Jun 8, 2026