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Procedure Products Syringes

FDA UDI

Class II (US FDA UDI)

by Procedure Products, Inc.

Identity

Trade Name
Procedure Products Syringes FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
3ml/cc Polycarbonate Syringe, White plunger, Luer-lock FDA UDI
Model / Reference
5003-W FDA UDI
Description
3ml/cc Polycarbonate Syringe, White plunger, Luer-lock FDA UDI

Identifiers

Catalog Number
5003-W FDA UDI
Primary DI / UDI-DI
B1605003W1 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

Category: General-purpose syringe, single-use

Procedure Products Syringes by Procedure Products, Inc. — 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

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Manufacturer

Sources (1)

  • FDA UDI c097f130-1fdd-483f-bfa8-7bc840514420 34 fields · synced Jun 8, 2026