Identity
- Trade Name
- ENDOSKELETON Posterior DPK FDA UDI
- Generic Name
- Orthopaedic joint/limb rongeur FDA UDI
- Device Name
- Kerrison Rongeur, 3mm, 8in Long FDA UDI
- Model / Reference
- 1100-0017 FDA UDI
- Description
- Kerrison Rongeur, 3mm, 8in Long FDA UDI
Identifiers
- Catalog Number
- 1100-0017 FDA UDI
- Primary DI / UDI-DI
- M682110000170 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic joint/limb rongeur FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Commercial Distribution
- Not 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
Dimensions & Sizes
- Size
- Length — 8 Inch FDA UDI
ENDOSKELETON Posterior DPK by Titan Spine, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Titan Spine, Inc.
Sources (1)
- FDA UDI 4264b97c-df47-4202-a2e9-b1814ee20c0a 37 fields · synced Jun 8, 2026