Identity
- Trade Name
- 25ga MaxReach Laser Probe EUDAMEDVortex Surgical Inc FDA UDI
- Generic Name
- Ophthalmic laser system beam guide FDA UDI
- Device Name
- Laser Probe and Illumination Devices EUDAMED25ga Max Reach Laser Probe Box of 5 FDA UDI25ga Flex-Tip Laser Probe FDA UDI
- Model / Reference
- VS0140.25 EUDAMEDFDA UDIVS0130.25 FDA UDI
- Description
- 25ga Max Reach Laser Probe Box of 5 FDA UDI25ga Flex-Tip Laser Probe FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810123480265 EUDAMEDFDA UDI00810123480289 FDA UDI
- Basic UDI-DI
- 081012348LaserDX EUDAMED
- Unit of Use DI
- 00810123480135 EUDAMED
- FDA Product Code
- HQB FDA UDI
- EMDN Code
- Q02040301 OCULAR ENDOPHOTOCOAGULATION FIBERS, SINGLE-USE EUDAMED
- GMDN Term
- Ophthalmic laser system beam guide FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 886.4690 FDA UDI
- Market of Registration
- Spain EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
25ga MaxReach Laser Probe by Vortex Surgical, Inc. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 081012348LaserDX | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Vortex Surgical Inc
- EUDAMED SRN
- US-MF-000022888
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (3)
- EUDAMED d74e9a05-69b9-42f9-9a15-5cbf5d1e9158 61 fields · synced Jul 29, 2026
- FDA UDI bd124d7e-d5e5-4d7e-a5a5-59f69765e34f 33 fields · synced May 30, 2026
- FDA UDI 4e243349-21b7-49df-b6d4-d932b331cbb3 33 fields · synced May 30, 2026