Identity
- Trade Name
- STILLE Bone Holding Forceps FDA UDI
- Generic Name
- Bone holding forceps FDA UDI
- Device Name
- BONE HOLDING FORCEPS SEMB STILLE 19.5 cm 7.75 in FDA UDI
- Model / Reference
- 105-16150 FDA UDI
- Description
- BONE HOLDING FORCEPS SEMB STILLE 19.5 cm 7.75 in FDA UDI
Identifiers
- Catalog Number
- 105-16150 FDA UDI
- Primary DI / UDI-DI
- 07332339211721 FDA UDI
- FDA Product Code
- HXP FDA UDI
- GMDN Term
- Bone holding forceps FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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 — 19.5 Centimeter FDA UDI
Category: Bone holding forceps
STILLE Bone Holding Forceps by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Bone holding forceps.
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- Novo Surgical — NOVO SURGICAL, INC. · Class I
- Tecomet — Tecomet,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 965cdba4-5000-48bc-878b-e163f806cd0c 36 fields · synced Jun 8, 2026