Double Dove

FDA UDI

Class II (US FDA UDI)

by Jumin Bio-Technologies, Co., Ltd.

Identity

Trade Name: Double Dove FDA UDI
Generic Name: General-purpose syringe/needle FDA UDI
Device Name: Sterile hypodermic syringe for single use, with needle, is intended to be used for medical purposes to inject fluid into or withdraw fluid from the body. Volume: 1mL; Needle size: 0.50*16mm RWLB; Nozzle type: Luer Lock. FDA UDI
Model / Reference: 0202 FDA UDI
Description: Sterile hypodermic syringe for single use, with needle, is intended to be used for medical purposes to inject fluid into or withdraw fluid from the body. Volume: 1mL; Needle size: 0.50*16mm RWLB; Nozzle type: Luer Lock. FDA UDI

Identifiers

Primary DI / UDI-DI: 06934755702022 FDA UDI
510(k) Number: K090929 FDA UDI
FDA Product Code: FMF FDA UDI
GMDN Term: General-purpose syringe/needle 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: General-purpose syringe/needle

Double Dove by Jumin Bio-Technologies, Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K090929 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Jumin Bio-Technologies, Co., Ltd.

Sources (1)

FDA UDI f0d996a8-48f6-4a3d-bd86-43a683cadea2 34 fields · synced May 31, 2026