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BladderScan®

FDA UDI

Class II (US FDA UDI)

by Verathon Inc.

Identity

Trade Name
BladderScan® FDA UDI
Generic Name
Bladder volume ultrasound imaging system FDA UDI
Model / Reference
BVI 6000 Series FDA UDI

Identifiers

Catalog Number
0270-0788 FDA UDI
Primary DI / UDI-DI
10879123004861 FDA UDI
510(k) Number
K022153 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Bladder volume ultrasound imaging system 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: Bladder volume ultrasound imaging system

BladderScan® by Verathon Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bladder volume ultrasound imaging system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Verathon Inc.

Sources (1)

  • FDA UDI 426026e3-f3e6-474c-bf7d-8ce2fca3dffa 34 fields · synced May 30, 2026