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Caina

FDA UDI

Class II (US FDA UDI)

by Jiangsu Caina Medical Co., Ltd

Identity

Trade Name
CAINA FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
The Syringe with permanently attached needle is intended for use by health care professionals for general purpose aspiration of fluid from vials, ampoules and liquid injection below the surface of the skin. FDA UDI
Model / Reference
0.5ML 28G*1/2" FDA UDI
Description
The Syringe with permanently attached needle is intended for use by health care professionals for general purpose aspiration of fluid from vials, ampoules and liquid injection below the surface of the skin. FDA UDI

Identifiers

Catalog Number
DC0152805 FDA UDI
Primary DI / UDI-DI
06971564466028 FDA UDI
510(k) Number
K192551 FDA UDI
FDA Product Code
FMF FDA UDI
MEG 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 — 0.5 Milliliter FDA UDI
Needle Gauge — 28 Gauge FDA UDI
Length — 0.5 Inch FDA UDI

Category: General-purpose syringe, single-use

Caina by Jiangsu Caina Medical Co., Ltd — 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

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Manufacturer

Sources (1)

  • FDA UDI 0c304e32-14ee-48ad-8de8-b746a239510e 36 fields · synced Jun 6, 2026