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Nurture Compression Pad

FDA UDI

Class I (US FDA UDI)

by Imalac, Inc.

Identity

Trade Name
Nurture Compression Pad FDA UDI
Generic Name
Breast pump, electric FDA UDI
Model / Reference
CP-00S-00-NU-L FDA UDI

Identifiers

Catalog Number
CP-00S-00-NU-L FDA UDI
Primary DI / UDI-DI
00850004882061 FDA UDI
FDA Product Code
PWA FDA UDI
GMDN Term
Breast pump, electric FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5150 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

Nurture Compression Pad by Imalac, Inc. — Class I — 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
Imalac, Inc.

Sources (1)

  • FDA UDI 905e8ef5-8f7c-4d38-a53a-41cd791cb497 33 fields · synced Jun 1, 2026