← Back to catalogue

Viverity

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Viverity FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
Single Electric Breast Pump FDA UDI
Model / Reference
ROS-SGEL FDA UDI
Description
Single Electric Breast Pump FDA UDI

Identifiers

Primary DI / UDI-DI
00092237612217 FDA UDI
FDA Product Code
HGX FDA UDI
GMDN Term
Breast pump, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5160 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

No

FDA UDI

Over-the-Counter

Yes

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: Breast pump, electric

Viverity by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breast pump, electric.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI dead588c-7541-4900-9f10-1285cbfb8f5b 34 fields · synced May 30, 2026