Identity
- Trade Name
- MIXOR FDA UDI
- Generic Name
- Manual orthopaedic cement mixer, reusable FDA UDI
- Device Name
- MIXOR PUMP ONLY FDA UDI
- Model / Reference
- 71270042 FDA UDI
- Description
- MIXOR PUMP ONLY FDA UDI
Identifiers
- Catalog Number
- 71270042 FDA UDI
- Primary DI / UDI-DI
- 03596010384607 FDA UDI
- FDA Product Code
- JDZ FDA UDI
- GMDN Term
- Manual orthopaedic cement mixer, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4210 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: Manual orthopaedic cement mixer, reusable
Mixor by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Manual orthopaedic cement mixer, reusable.
- Pro Nozzle medium — Heraeus Medical LLC · Class I
- ACM — Stryker Corp. · Class I
- Henry Schein — HENRY SCHEIN, INC. · Class I
- PCD — Stryker Corp. · Class II
- ACM — Stryker Corp. · Class I
- MixEvac — Stryker Corp. · Class I
- Howmedica, Mix-Kit — Stryker Corp. · Class I
- PCD SpinePlex — Stryker Corp. · Class II
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
- Smith & Nephew, Inc.
Sources (1)
- FDA UDI 0d8e7ba8-6521-46cb-ac5d-516404d21146 35 fields · synced Jun 8, 2026