← Back to catalogue

CarePoint Precision

FDA UDI

Class II (US FDA UDI)

by Allison Medical, Inc.

Identity

Trade Name
CarePoint Precision FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
10mL Luer Lock Syringe FDA UDI
Model / Reference
04-0010 FDA UDI
Description
10mL Luer Lock Syringe FDA UDI

Identifiers

Primary DI / UDI-DI
00786227041056 FDA UDI
510(k) Number
K124037 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

Dimensions & Sizes

Size
Total Volume — 10 Milliliter FDA UDI

Category: General-purpose syringe, single-use

CarePoint Precision by Allison Medical, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 99e50272-1e3c-4386-9f89-c7b0a95c8fe9 35 fields · synced May 30, 2026