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Lifemed Male to Male Luer Adapter

FDA UDI

Class II (US FDA UDI)

by Lifemed of California

Identity

Trade Name
Lifemed Male to Male Luer Adapter FDA UDI
Generic Name
Haemodialysis blood tubing set, single-use FDA UDI
Device Name
Male to Male Luer Adapter FDA UDI
Model / Reference
B3109Z FDA UDI
Description
Male to Male Luer Adapter FDA UDI

Identifiers

Catalog Number
B3109Z FDA UDI
Primary DI / UDI-DI
00852250006048 FDA UDI
FDA Product Code
FJK FDA UDI
GMDN Term
Haemodialysis blood tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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: Haemodialysis blood tubing set, single-use

Lifemed Male to Male Luer Adapter by Lifemed of California — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Haemodialysis blood tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fb72315a-8e58-44ee-933c-0870b1cb546b 36 fields · synced Jun 6, 2026