Identity
- Trade Name
- STILLE Osteotomes FDA UDI
- Generic Name
- Orthopaedic osteotome FDA UDI
- Device Name
- HAND OSTEOTOME STILLE 8 mm curved blade R45 mm phenolic handle 16 cm 6.25 in FDA UDI
- Model / Reference
- 100-111-0083 FDA UDI
- Description
- HAND OSTEOTOME STILLE 8 mm curved blade R45 mm phenolic handle 16 cm 6.25 in FDA UDI
Identifiers
- Catalog Number
- 100-111-0083 FDA UDI
- Primary DI / UDI-DI
- 07332339232931 FDA UDI
- FDA Product Code
- KDG FDA UDI
- GMDN Term
- Orthopaedic osteotome FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 16 Centimeter FDA UDI
Category: Orthopaedic osteotome
STILLE Osteotomes by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic osteotome.
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- ORTHOMED — ORTHO-MED, INC. · Class I
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
- Stille AB
Sources (1)
- FDA UDI 3a62a37d-6682-45a8-8519-e78f29d84720 36 fields · synced May 31, 2026