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Aquilavie

FDA UDI

Class II (US FDA UDI)

by Ahc Americas LLC

Identity

Trade Name
AQUILAVIE FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
Sterile Disposable Safety Needle, 18Gx1-1/2" (1.2mm x 38mm), 100pcs/box, 20boxes/carton FDA UDI
Model / Reference
J10047 FDA UDI
Description
Sterile Disposable Safety Needle, 18Gx1-1/2" (1.2mm x 38mm), 100pcs/box, 20boxes/carton FDA UDI

Identifiers

Catalog Number
J10047 FDA UDI
Primary DI / UDI-DI
10810118890588 FDA UDI
FDA Product Code
MEG FDA UDI
FMF FDA UDI
FMI FDA UDI
GMDN Term
Hypodermic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
880.5570 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

Yes

FDA UDI

Category: Hypodermic needle, single-use

Aquilavie by Ahc Americas LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ahc Americas LLC

Sources (1)

  • FDA UDI ad21bb4d-006e-48ba-a3e8-fca6746acc39 34 fields · synced May 30, 2026