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Healix Awl
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 222223Model General Orthopedic Use Awls, Taps, and Reamers
Identity
- Trade Name
- HEALIX AWL EUDAMEDFDA UDI
- Generic Name
- Bone awl, reusable FDA UDI
- Device Name
- Awl, Tap, Reamer, Femoral, Tibial, Cortical, Arthroscopic, Healix, Healix Advance, GII, Gryphon, Milagro EUDAMEDHEALIX Awl FDA UDI
- Model / Reference
- 222223 EUDAMEDFDA UDIGeneral Orthopedic Use Awls, Taps, and Reamers EUDAMED
- Description
- HEALIX Awl FDA UDI
Identifiers
- Catalog Number
- 222223 FDA UDI
- Primary DI / UDI-DI
- 10886705007707 EUDAMEDFDA UDI
- Basic UDI-DI
- 0886705a00121K4 EUDAMED
- Direct Marketing DI
- 10886705007707 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Bone awl, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 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 awl, reusable
Healix Awl by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Bone awl, reusable.
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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 |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (2)
- FDA UDI e72c95b1-1cbd-4ba9-bf5f-04de121bbb57 35 fields · synced Jul 21, 2026
- EUDAMED fbc28641-1f81-44b6-b1b2-75e92ec2c890 61 fields · synced Jul 21, 2026