Identity
- Trade Name
- HYGITECH FDA UDI
- Generic Name
- Bone cutter FDA UDI
- Device Name
- US3 surgery tip compatible Mectron HYGITECH Reference: HY-98015 Flat scalpel for very precise cutting of bone in thinanatomical structures. All high-precisionosteotomy techniques such as crest expansion, interdental corticotomies, non-traumatic nasal spine. FDA UDI
- Model / Reference
- HY-98015 FDA UDI
- Description
- US3 surgery tip compatible Mectron HYGITECH Reference: HY-98015 Flat scalpel for very precise cutting of bone in thinanatomical structures. All high-precisionosteotomy techniques such as crest expansion, interdental corticotomies, non-traumatic nasal spine. FDA UDI
Identifiers
- Catalog Number
- HY-98015 FDA UDI
- Primary DI / UDI-DI
- 03615140005753 FDA UDI
- FDA Product Code
- EJB FDA UDI
- GMDN Term
- Bone cutter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Bone cutter
Hygitech by Hygitech — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Hygitech
Sources (1)
- FDA UDI 55c7a109-b660-4cc1-a580-277b678f9f81 34 fields · synced Jun 1, 2026