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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
Electronic gravity infusion controller administration set FDA UDI
Device Name
27GA, 6mm, 24" Single Lumen Safety Subcutaneous Tissue Infusion Set with Transparent dressing, Latex Free, Non-DEHP PVC tubing, Priming Volume Approx: .15ml FDA UDI
Model / Reference
MC2406-SS FDA UDI
Description
27GA, 6mm, 24" Single Lumen Safety Subcutaneous Tissue Infusion Set with Transparent dressing, Latex Free, Non-DEHP PVC tubing, Priming Volume Approx: .15ml FDA UDI

Identifiers

Primary DI / UDI-DI
10816339020018 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Electronic gravity infusion controller administration 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: Electronic gravity infusion controller administration 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 Electronic gravity infusion controller administration 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 2a1607e8-a4ac-481f-ba8e-8bf13f2e76a0 34 fields · synced May 30, 2026