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Dar

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
DAR FDA UDI
Generic Name
Y-piece breathing circuit connector, single-use FDA UDI
Device Name
L Connector Double Swivel FDA UDI
Model / Reference
610U5257 FDA UDI
Description
L Connector Double Swivel FDA UDI

Identifiers

Primary DI / UDI-DI
10884521854147 FDA UDI
FDA Product Code
BZA FDA UDI
GMDN Term
Y-piece breathing circuit connector, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5810 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Y-piece breathing circuit connector, single-use

Dar by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Y-piece breathing circuit connector, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 12ed4d11-7c8a-4b61-b2bf-10c3d3953f1f 36 fields · synced Jun 1, 2026