Identity
- Trade Name
- Mill Plus FDA UDI
- Generic Name
- Powered bone mill cartridge FDA UDI
- Device Name
- Medium Blade FDA UDI
- Model / Reference
- 5420MED000 FDA UDI
- Description
- Medium Blade FDA UDI
Identifiers
- Catalog Number
- 5420-MED-000 FDA UDI
- Primary DI / UDI-DI
- 07613327539332 FDA UDI
- FDA Product Code
- HWE FDA UDI
- GMDN Term
- Powered bone mill cartridge FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4820 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
Yes
FDA UDI
Category: Powered bone mill cartridge
Mill Plus by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Powered bone mill cartridge.
- Bone Shark® — Tarca LLC · Class I
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- Medtronic — Provision · Class I
- Prep Plus — Stryker Corp. · Class I
- Mill Plus — Stryker Corp. · Class I
- Mill Plus — Stryker Corp. · 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
- Stryker Corp.
Sources (1)
- FDA UDI 98093949-79cf-4e41-b959-e1462b6dca8b 35 fields · synced Jun 8, 2026