Identity
- Trade Name
- BladderScan® FDA UDI
- Generic Name
- Ultrasound system quality assurance device FDA UDI
- Model / Reference
- Pediatric Phantom FDA UDI
Identifiers
- Catalog Number
- 0620-0273 FDA UDI
- Primary DI / UDI-DI
- 00879123006172 FDA UDI
- FDA Product Code
- IYO FDA UDI
- GMDN Term
- Ultrasound system quality assurance device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1560 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
Category: Ultrasound system quality assurance device
BladderScan® by Verathon Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ultrasound system quality assurance device.
- BladderScan® — Verathon Inc. · Class II
- BladderScan® — Verathon Inc. · Class II
- BladderScan® — Verathon Inc. · Class II
- BladderScan® — Verathon Inc. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Verathon Inc.
Sources (1)
- FDA UDI cbfb07fa-b60b-40d3-a196-01ddf8e5134e 33 fields · synced May 30, 2026