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Medpoint

FDA UDI

Class II (US FDA UDI)

by Carelife (usa) Inc.

Identity

Trade Name
Medpoint FDA UDI
Generic Name
Insulin syringe/needle, safety FDA UDI
Device Name
Safety insulin syringe 1ML 29Gx1/2" FDA UDI
Model / Reference
1 FDA UDI
Description
Safety insulin syringe 1ML 29Gx1/2" FDA UDI

Identifiers

Catalog Number
08-01-2905S FDA UDI
Primary DI / UDI-DI
M99208012905S3 FDA UDI
510(k) Number
K191639 FDA UDI
FDA Product Code
MEG FDA UDI
GMDN Term
Insulin syringe/needle, safety 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

Yes

FDA UDI

Category: Insulin syringe/needle, safety

Medpoint by Carelife (usa) Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Insulin syringe/needle, safety.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Carelife (usa) Inc.

Sources (1)

  • FDA UDI e35cb8e0-589d-4f96-946a-db0bf52cd77f 36 fields · synced Jun 1, 2026