Identity
- Trade Name
- FullFire® Diffusing Tip Laser Probe FDA UDI
- Generic Name
- MRI-guided laser interstitial thermal therapy system beam guide FDA UDI
- Device Name
- 3.3mm Diffusing Tip Laser Probe FDA UDI
- Model / Reference
- 20414-1 FDA UDI
- Description
- 3.3mm Diffusing Tip Laser Probe FDA UDI
Identifiers
- Catalog Number
- DTP-101-01 FDA UDI
- Primary DI / UDI-DI
- 00816589020533 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- MRI-guided laser interstitial thermal therapy system beam guide FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
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 Conditional FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 3.3 Millimeter FDA UDI
FullFire® Diffusing Tip Laser Probe by Monteris Medical Corp — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Monteris Medical Corp
Sources (1)
- FDA UDI 87d7f451-c38c-4a07-909c-700d60e76795 37 fields · synced May 30, 2026