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MF 200 Series
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref MF-200/240-A-DTModel MF 200 Series
Identity
- Trade Name
- MF 200 Series EUDAMEDMF-200/240-A-DT FDA UDI
- Generic Name
- General/multiple surgical laser system beam guide, reusable FDA UDI
- Device Name
- MF-200/240-A-DT EUDAMEDSurgical Laser Fiber 200/240/400, hard clad, blue tefzel, NA 0.22, Absorbing Dark Hole Connector® SMA905 , single use, silver extension sleeves, EO sterile, Dome Tip, MF label FDA UDI
- Model / Reference
- MF 200 Series EUDAMEDMF-200/240-A-DT EUDAMEDFDA UDI
- Description
- Surgical Laser Fiber 200/240/400, hard clad, blue tefzel, NA 0.22, Absorbing Dark Hole Connector® SMA905 , single use, silver extension sleeves, EO sterile, Dome Tip, MF label FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00855950006127 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00855950006127 EUDAMED
- 510(k) Number
- K124003 FDA UDI
- FDA Product Code
- GEX FDA UDI
- EMDN Code
- Z12011003 HOLMIUM SURGICAL LASER EUDAMED
- GMDN Term
- General/multiple surgical laser system beam guide, reusable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Market of Registration
- Germany 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
MF 200 Series by Med -fibers Inc. — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00855950006127 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- MED-Fibers, Inc.
- EUDAMED SRN
- US-MF-000039524
- Authorised Representative
- Total-Laser Solution GmbH AT-AR-000021498
Sources (2)
- EUDAMED 308753dd-7237-4069-906b-20febd9391d8 61 fields · synced Jul 16, 2026
- FDA UDI 07bad29b-4e5c-45ed-91b7-dc3931b0cc53 34 fields · synced May 25, 2026