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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
9" Bifurcated Extension set with Male Luer Lock Pinch Clamps and 2 Female Luer Locks. Lipid Resistant, Non-DEHP PVC tubing, Latex Free. Approximate Priming Volume 0.6ml FDA UDI
Model / Reference
40-0902 FDA UDI
Description
9" Bifurcated Extension set with Male Luer Lock Pinch Clamps and 2 Female Luer Locks. Lipid Resistant, Non-DEHP PVC tubing, Latex Free. Approximate Priming Volume 0.6ml FDA UDI

Identifiers

Primary DI / UDI-DI
10816339022081 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

No

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

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Manufacturer

Manufacturer
All-Med Inc

Sources (1)

  • FDA UDI 4f0d4ff9-553a-4da4-a849-ba690b39ebfa 34 fields · synced May 30, 2026