← Back to catalogue

All-Med, Inc.

FDA UDI

Class II (US FDA UDI)

by All-Med Inc

Identity

Trade Name
All-Med, Inc. FDA UDI
Generic Name
Intravenous administration tubing extension set FDA UDI
Device Name
45" Pump Extension Set with two Male Luer Locks and Slide Clamp. Lipid Resistant, Non-DEHP PVC tubing, Latex Free. Approximate Priming Volume: 1.4ml FDA UDI
Model / Reference
42-4500 FDA UDI
Description
45" Pump Extension Set with two Male Luer Locks and Slide Clamp. Lipid Resistant, Non-DEHP PVC tubing, Latex Free. Approximate Priming Volume: 1.4ml FDA UDI

Identifiers

Primary DI / UDI-DI
10816339022340 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Intravenous administration tubing extension set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

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: Intravenous administration tubing extension set

All-Med, Inc. by All-Med Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration tubing extension set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
All-Med Inc

Sources (1)

  • FDA UDI 3d8f731a-d727-4b2b-981f-a7cbe30e9151 34 fields · synced Jun 1, 2026