Identity
- Trade Name
- Quadcut FDA UDI
- Generic Name
- Metal/carbide ENT bur, single-use FDA UDI
- Device Name
- BLADE 1884080EM TRICUT 4MMX13CM M4 ROHS FDA UDI
- Model / Reference
- 1884080EM FDA UDI
- Description
- BLADE 1884080EM TRICUT 4MMX13CM M4 ROHS FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000579241 FDA UDI
- FDA Product Code
- HAW FDA UDI
- GMDN Term
- Metal/carbide ENT bur, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4560 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 4.0 Millimeter FDA UDILength — 13.0 Centimeter FDA UDI
Category: Metal/carbide ENT bur, single-use
Quadcut by Medtronic Xomed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Medtronic Xomed, Inc.
Sources (1)
- FDA UDI c6f0f79f-5ebe-4d87-9501-8f05e91891b2 35 fields · synced May 31, 2026