Nipro Disposable Syringe

FDA UDI

Class II (US FDA UDI)

by Nipro Medical Corporation

Identity

Trade Name: NIPRO DISPOSABLE SYRINGE FDA UDI
Generic Name: General-purpose syringe, single-use FDA UDI
Device Name: 1mL x 25G 5/8" FDA UDI
Model / Reference: JD+01D2516-WEI FDA UDI
Description: 1mL x 25G 5/8" FDA UDI

Identifiers

Primary DI / UDI-DI: 00383790008235 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

Dimensions & Sizes

Size: Total Volume — 1 Milliliter FDA UDI
Length — 0.625 Inch FDA UDI
Needle Gauge — 25 Gauge FDA UDI

Category: General-purpose syringe, single-use

Nipro Disposable Syringe by Nipro Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as General-purpose syringe, single-use.

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HSW HENKE-JECT® — Henke-Sass, Wolf GmbH · Class II
BD Safety-Lok — BECTON DICKINSON AND COMPANY · Class II
SURGYCO — Surgyco LLC · Class I

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: Nipro Medical Corporation

Sources (1)

FDA UDI 67ef261f-280e-4a32-b129-b14c678ef274 35 fields · synced Jun 1, 2026