← Back to catalogue

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
50mL Luer Lock without Needle FDA UDI
Model / Reference
JD+50L-WEI FDA UDI
Description
50mL Luer Lock without Needle FDA UDI

Identifiers

Primary DI / UDI-DI
00383790008754 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 — 50 Milliliter 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

Similar devices

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

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 5087d6c7-5952-42bb-a434-51ce9dec2eba 35 fields · synced Jun 1, 2026