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Care One

FDA UDI

Class II (US FDA UDI)

by Ahold U.S.A., Inc.

Identity

Trade Name
Care One FDA UDI
Generic Name
Autoinjector needle FDA UDI
Device Name
4mm 33G Pen Needle with Remover- Unifine Pentips Plus FDA UDI
Model / Reference
AN 3860AH FDA UDI
Description
4mm 33G Pen Needle with Remover- Unifine Pentips Plus FDA UDI

Identifiers

Primary DI / UDI-DI
00341520005879 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

Category: Autoinjector needle

Care One 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 ef848094-edb8-4f1e-ab9e-571f0983dc53 34 fields · synced May 30, 2026