← Back to catalogue
Clearfix
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 253111Model General Orthopedic Use Probes
Identity
- Trade Name
- CLEARFIX Meniscal Rasp EUDAMEDCLEARFIX FDA UDI
- Generic Name
- Bone file/rasp, manual, reusable FDA UDI
- Device Name
- Meniscal Rasp, Straight Up, Straight, 45 Degree, 90 Degree EUDAMEDCLEARFIX Meniscal Rasp Straight-Up / 90 Degrees Face FDA UDI
- Model / Reference
- 253111 EUDAMEDFDA UDIGeneral Orthopedic Use Probes EUDAMED
- Description
- CLEARFIX Meniscal Rasp Straight-Up / 90 Degrees Face FDA UDI
Identifiers
- Catalog Number
- 253111 FDA UDI
- Primary DI / UDI-DI
- 10886705012626 EUDAMEDFDA UDI
- Basic UDI-DI
- 0886705a00131K7 EUDAMED
- Direct Marketing DI
- 10886705012626 EUDAMED
- FDA Product Code
- NBH FDA UDI
- EMDN Code
- L1920 ARTHROSCOPIC SURGERY FILES AND RASPS, REUSABLE EUDAMED
- GMDN Term
- Bone file/rasp, manual, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.1100 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
Yes
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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone file/rasp, manual, reusable
Clearfix by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Bone file/rasp, manual, reusable.
- Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
- NORDENT MANUFACTURING INC — NORDENT MANUFACTURING INC · Class I
- Life Instruments — Life Instrument Corporation · Class I
- TALOS®-C — MEDITECH SPINE, LLC · Class II
- DeGen Standard Instrumentation — Degen Medical · Class I
- TiWave C Cervical Cage System — Kalitec Direct LLC · Class I
- BOSS Instruments — Boss Instruments, Ltd. · Class I
- 4WEB Medical — 4Web Medical, Inc. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (2)
- FDA UDI 96699309-4439-4b92-b53c-1375cf799cae 35 fields · synced Jul 9, 2026
- EUDAMED c3a26978-2905-4617-8fe9-f96772923517 61 fields · synced Jul 9, 2026