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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
24" Subcutaneous Needle Winged Infusion Set, 27ga. 30 degree bent needle, female luer lock, Non-DEHP PVC tubing, Latex Free, Lipid Resistant. Approx. Priming Volume 0.12ml FDA UDI
Model / Reference
59-2724 FDA UDI
Description
24" Subcutaneous Needle Winged Infusion Set, 27ga. 30 degree bent needle, female luer lock, Non-DEHP PVC tubing, Latex Free, Lipid Resistant. Approx. Priming Volume 0.12ml FDA UDI

Identifiers

Primary DI / UDI-DI
10816339020469 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

No

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 3e810c93-e6a5-4580-aebd-ef3b140c179c 34 fields · synced May 31, 2026