Identity
- Trade Name
- Sonopet iQ FDA UDI
- Generic Name
- Hard/soft-tissue ultrasonic surgical system handpiece FDA UDI
- Device Name
- Universal Angled Handpiece FDA UDI
- Model / Reference
- 5500255000 FDA UDI
- Description
- Universal Angled Handpiece FDA UDI
Identifiers
- Catalog Number
- 5500-255-000 FDA UDI
- Primary DI / UDI-DI
- 07613327298611 FDA UDI
- FDA Product Code
- LFL FDA UDI
- GMDN Term
- Hard/soft-tissue ultrasonic surgical system handpiece 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
Moist Heat or Steam Sterilization FDA UDI
MR Unsafe FDA UDI
Category: Hard/soft-tissue ultrasonic surgical system handpiece
Sonopet iQ by Stryker Corp. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 611ebbc8-4414-4ee2-bdc2-f43b4abfc6f9 36 fields · synced Jun 8, 2026