Identity
- Trade Name
- Surgical Instrument FDA UDI
- Generic Name
- Orthopaedic bone pin container FDA UDI
- Model / Reference
- 111-224-B FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08800089452675 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Orthopaedic bone pin container FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Orthopaedic bone pin container
Surgical Instrument by Jeil Medical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Orthopaedic bone pin container.
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- K-Wire and Steinmann Pin Dispensers — Key Surgical, LLC · Class I
- Newclip Instruments — NEWCLIP TECHNICS · Class I
- LEOS Cannulated Screw System — Tyber Medical · Class I
- gSource — GSOURCE, LLC. · 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
- Jeil Medical Corporation
Sources (1)
- FDA UDI 643fe5f8-51aa-4496-8137-9d009c9d1d81 32 fields · synced May 30, 2026