Identity
- Trade Name
- Sonopet iQ FDA UDI
- Generic Name
- Ultrasonic surgical system generator FDA UDI
- Device Name
- Advanced Foot Pedal FDA UDI
- Model / Reference
- 5500007000 FDA UDI
- Description
- Advanced Foot Pedal FDA UDI
Identifiers
- Catalog Number
- 5500-007-000 FDA UDI
- Primary DI / UDI-DI
- 07613327298659 FDA UDI
- FDA Product Code
- LFL FDA UDI
- GMDN Term
- Ultrasonic surgical system generator FDA UDI
Classification
- Device Class
- U 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Ultrasonic surgical system generator
Sonopet iQ by Stryker Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Irrigation sleeve — Beijing Sonicmed Technologies Co., Ltd. · Class IIa
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 U | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI a27c7a9b-8316-49c0-91aa-2583ed22032d 36 fields · synced May 30, 2026