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Curos™

FDA UDI

Class U (US FDA UDI)

by 3m Company

Identity

Trade Name
Curos™ FDA UDI
Generic Name
Luer-formatted disinfection cap FDA UDI
Device Name
3M™ Curos™ open female luer cap teal 5 each/strip 50 Strips/carton 8 Cartons/Case CSV5-250 FDA UDI
Model / Reference
CSV5-250 FDA UDI
Description
3M™ Curos™ open female luer cap teal 5 each/strip 50 Strips/carton 8 Cartons/Case CSV5-250 FDA UDI

Identifiers

Catalog Number
CSV5-250 FDA UDI
Primary DI / UDI-DI
30707387781034 FDA UDI
FDA Product Code
LKB FDA UDI
GMDN Term
Luer-formatted disinfection cap FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Luer-formatted disinfection cap

Curos™ by 3m Company — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted disinfection cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3m Company

Sources (1)

  • FDA UDI ed830c10-9862-448a-8a5b-16c8a8c4e211 35 fields · synced May 30, 2026