Identity
- Trade Name
- PhotonGuide XT System FDA UDI
- Generic Name
- Surgical instrument fibreoptic light FDA UDI
- Device Name
- The PhotonGuide XT System is intended to provide surgical site illumination from a high intensity light source. FDA UDI
- Model / Reference
- Narrow / Angled FDA UDI
- Description
- The PhotonGuide XT System is intended to provide surgical site illumination from a high intensity light source. FDA UDI
Identifiers
- Catalog Number
- 104001XT FDA UDI
- Primary DI / UDI-DI
- 00816728020110 FDA UDI
- FDA Product Code
- FDG FDA UDI
- GMDN Term
- Surgical instrument fibreoptic light FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4530 FDA UDI
- Commercial Distribution
- Not 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
PhotonGuide XT System by Invuity, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
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Manufacturer
- Manufacturer
- Invuity, Inc.
Sources (1)
- FDA UDI c16a5c0d-924b-4047-81db-bddda2b4bcd9 37 fields · synced Jun 8, 2026