Identity
- Trade Name
- SPATULA FDA UDI
- Generic Name
- Brain spatula FDA UDI
- Device Name
- BRAIN, OLIVECRONA, DOUBLE ENDED, CONVEX, 7/9 MM TIPS FDA UDI
- Model / Reference
- 24-713-18-01 FDA UDI
- Description
- BRAIN, OLIVECRONA, DOUBLE ENDED, CONVEX, 7/9 MM TIPS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00888118033536 FDA UDI
- FDA Product Code
- GAF FDA UDI
- GMDN Term
- Brain spatula 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Brain spatula
Spatula by KLS-Martin L.P. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Brain spatula.
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- Sklar — Sklar Corporation · Class I
- LAZIC — Peter Lazic GmbH · Class I
- Ambler Surgical — Ambler Surgical, LLC · Class I
- PILLING — TELEFLEX INCORPORATED · Class I
- MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
- Sklar — Sklar Corporation · Class I
- LAZIC — Peter Lazic GmbH · 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
- KLS-Martin L.P.
Sources (1)
- FDA UDI 7b3a6008-2998-4d61-948f-83b6ee9ee9de 35 fields · synced Jun 8, 2026