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TensCare

FDA UDI

Class II (US FDA UDI)

by Tenscare Limited

Identity

Trade Name
TensCare FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
The Nouri Digital Electric Breast Pump is a powered breast pump to be used by lactating women to express and collect milk from their breasts. It is intended for a single user. FDA UDI
Model / Reference
Nouri Duo FDA UDI
Description
The Nouri Digital Electric Breast Pump is a powered breast pump to be used by lactating women to express and collect milk from their breasts. It is intended for a single user. FDA UDI

Identifiers

Catalog Number
K00147 FDA UDI
Primary DI / UDI-DI
05033435135776 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

Yes

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

TensCare by Tenscare Limited — 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

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Manufacturer

Manufacturer
Tenscare Limited

Sources (1)

  • FDA UDI 50c318f8-ab3e-4391-a47b-194851fbc4ee 34 fields · synced Jun 6, 2026