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Allied Medical LLC

FDA UDI

Class II (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
Allied Medical LLC FDA UDI
Generic Name
Vacuum quick-connect coupling, female FDA UDI
Device Name
Fitting FDA UDI
Model / Reference
S165-306-001 FDA UDI
Description
Fitting FDA UDI

Identifiers

Catalog Number
22-11-0102 FDA UDI
Primary DI / UDI-DI
00026072002810 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Vacuum quick-connect coupling, female FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vacuum quick-connect coupling, female

Allied Medical LLC by Allied Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum quick-connect coupling, female.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI e66efd61-21b4-490e-b449-06bc5c53fa2b 34 fields · synced Jun 6, 2026