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Curity

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Curity FDA UDI
Generic Name
Nipple pad/ring, single-use FDA UDI
Device Name
Nursing Pad,Moderate FDA UDI
Model / Reference
2630 FDA UDI
Description
Nursing Pad,Moderate FDA UDI

Identifiers

Catalog Number
2630 FDA UDI
Primary DI / UDI-DI
10884527006922 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Nipple pad/ring, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5 Inch FDA UDI

Category: Nipple pad/ring, single-use

Curity by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nipple pad/ring, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 0bc9f8da-1e31-432f-bf17-57624ec47f5f 37 fields · synced May 29, 2026