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Ahs

FDA UDI

Class II (US FDA UDI)

by American Health Service Sales Corporation

Identity

Trade Name
AHS FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
SYRINGE,3CC,LUER LOCK,22 X 1.5 FDA UDI
Model / Reference
AH03L2238 FDA UDI
Description
SYRINGE,3CC,LUER LOCK,22 X 1.5 FDA UDI

Identifiers

Primary DI / UDI-DI
B031AH03L22380 FDA UDI
510(k) Number
K050999 FDA UDI
K112057 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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: General-purpose syringe, single-use

Ahs by American Health Service Sales Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose syringe, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 566be868-789b-4a8a-96b4-cef62aa325f6 34 fields · synced May 30, 2026