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Ahold - CareOne UPP 8mm pen needles

FDA UDI

Class II (US FDA UDI)

by Ahold U.S.A., Inc.

Identity

Trade Name
Ahold - CareOne UPP 8mm pen needles FDA UDI
Generic Name
Autoinjector needle FDA UDI
Device Name
For use with injectors for the subcutaneous injection of approved drugs, including insulin FDA UDI
Model / Reference
AN 3830AH FDA UDI
Description
For use with injectors for the subcutaneous injection of approved drugs, including insulin FDA UDI

Identifiers

Catalog Number
AN 3830AH FDA UDI
Primary DI / UDI-DI
00041520035387 FDA UDI
510(k) Number
K152339 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Autoinjector needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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

Yes

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

Dimensions & Sizes

Size
Length — 8 Millimeter FDA UDI
Needle Gauge — 31 Gauge FDA UDI

Category: Autoinjector needle

Ahold - CareOne UPP 8mm pen needles by Ahold U.S.A., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autoinjector needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ahold U.S.A., Inc.

Sources (1)

  • FDA UDI a01b0b16-1c50-4956-875f-03b955c97f03 38 fields · synced Jun 1, 2026