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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
Hypodermic needle, single-use FDA UDI
Device Name
Disposable Needle 23Gx1”.Needles are intended to be used with a legally marketed syringe intend to inject fluids into or withdraw fluids from the body. FDA UDI
Model / Reference
23G×1 FDA UDI
Description
Disposable Needle 23Gx1”.Needles are intended to be used with a legally marketed syringe intend to inject fluids into or withdraw fluids from the body. FDA UDI

Identifiers

Catalog Number
SN10012 FDA UDI
Primary DI / UDI-DI
06971564465274 FDA UDI
510(k) Number
K113091 FDA UDI
FDA Product Code
FMI FDA UDI
FMF FDA UDI
GMDN Term
Hypodermic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 FDA UDI
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
Needle Gauge — 23 Gauge FDA UDI
Length — 1 Inch FDA UDI

Category: Hypodermic needle, 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 Hypodermic needle, 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 62b63247-1a0e-4b1f-b482-621790eabb68 36 fields · synced May 31, 2026