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Syringes Safety

FDA UDI

Class II (US FDA UDI)

by Geri-Gentle Corporation

Identity

Trade Name
Syringes Safety FDA UDI
Generic Name
General-purpose syringe, single-use FDA UDI
Device Name
SYR U100 .5cc 29x.5 FDA UDI
Model / Reference
11467 FDA UDI
Description
SYR U100 .5cc 29x.5 FDA UDI

Identifiers

Primary DI / UDI-DI
10369771000907 FDA UDI
FDA Product Code
MEG 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: General-purpose syringe, single-use

Syringes Safety by Geri-Gentle 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

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Manufacturer

Sources (1)

  • FDA UDI 8b054c29-dc96-4aa1-8269-2a114bce2893 33 fields · synced May 30, 2026