Identity
- Trade Name
- Discectomy Set FDA UDI
- Generic Name
- Orthopaedic cement curette FDA UDI
- Device Name
- 5x7.5mm 45 degree Rev Angle Curette FDA UDI
- Model / Reference
- 15-02-09 FDA UDI
- Description
- 5x7.5mm 45 degree Rev Angle Curette FDA UDI
Identifiers
- Catalog Number
- 303-0114 FDA UDI
- Primary DI / UDI-DI
- M7403030114 FDA UDI
- FDA Product Code
- LXH FDA UDI
- GMDN Term
- Orthopaedic cement curette 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
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Orthopaedic cement curette
Discectomy Set by Spineology Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Discectomy Set — SPINEOLOGY INC. · Class I
- Discectomy Set — SPINEOLOGY 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
- Spineology Inc.
Sources (1)
- FDA UDI cdda7bcc-0962-47c7-bfee-f6530c6ff30d 35 fields · synced Jun 6, 2026