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Luer Lock Disc Filter (male To Female)

FDA UDI

Class I (US FDA UDI)

by Flexicare Medical Limited

Identity

Trade Name
LUER LOCK DISC FILTER (MALE TO FEMALE) FDA UDI
Generic Name
Hydrophobic Luer filter FDA UDI
Model / Reference
010-742U FDA UDI

Identifiers

Primary DI / UDI-DI
05055788716778 FDA UDI
FDA Product Code
JRL FDA UDI
GMDN Term
Hydrophobic Luer filter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2050 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

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: Hydrophobic Luer filter

Luer Lock Disc Filter (male To Female) by Flexicare Medical Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hydrophobic Luer filter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2243fc57-5476-40d9-aef5-3a7d30514876 32 fields · synced May 30, 2026