Identity
- Trade Name
- MF-272/300-SD-Flexx FDA UDI
- Generic Name
- General/multiple surgical laser system beam guide, reusable FDA UDI
- Device Name
- Surgical Laser Fiber , 272/300/450, silicone, blue tefzel, NA 0.22, Superdry Connector® SMA 905, Flexx Trak™ Ball Tip, single use, extension sleeve, EO sterile, label FDA UDI
- Model / Reference
- MF-272/300-SD-Flexx FDA UDI
- Description
- Surgical Laser Fiber , 272/300/450, silicone, blue tefzel, NA 0.22, Superdry Connector® SMA 905, Flexx Trak™ Ball Tip, single use, extension sleeve, EO sterile, label FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00855950006301 FDA UDI
- 510(k) Number
- K124003 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- General/multiple surgical laser system beam guide, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General/multiple surgical laser system beam guide, reusable
MF-272/300-SD-Flexx by Med -fibers Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as General/multiple surgical laser system beam guide, reusable.
- ProFlex — INNOVAQUARTZ LLC · Class II
- Accu-Beam — Transamerican Technologies International · Class II
- Accu-Beam — Transamerican Technologies International · Class II
- Flex-G Laser Fiber with Extended Length Sheath — OPTICAL INTEGRITY, INC. · Class II
- ProFlex — INNOVAQUARTZ LLC · Class II
- Q-Lase™ Side-Firing Laser Fiber with SMA Connector — OPTICAL INTEGRITY, INC. · Class II
- Laser Applicator Non-cooled Instructions for Use — Clinical Laserthermia Systems AB · Class II
- Twister — WISDOM MEDICAL TECHNOLOGY, LLC · Class II
Cleared under the same submission
K124003 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 |
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Manufacturer
- Manufacturer
- Med -fibers Inc.
Sources (1)
- FDA UDI 24f54623-116f-4532-b6df-0111ade69cb4 34 fields · synced May 30, 2026