Hypodermic Needles, Non-Toxic, 23G x 1"

FDA UDI

Class II (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Hypodermic Needles, Non-Toxic, 23G x 1" FDA UDI
Generic Name: Hypodermic needle, single-use FDA UDI
Device Name: Sterile-Eo FDA UDI
Model / Reference: 6970 FDA UDI
Description: Sterile-Eo FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784697024 FDA UDI
FDA Product Code: FMI FDA UDI
FMF FDA UDI
MEG FDA UDI
GMDN Term: Hypodermic needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5570 FDA UDI
880.5860 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

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

Yes

FDA UDI

Category: Hypodermic needle, single-use

Hypodermic Needles, Non-Toxic, 23G x 1" by Dynarex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Dynarex Corp.

Sources (1)

FDA UDI 63852d58-7e6b-4c7f-a572-35ecbe66c46f 33 fields · synced Jun 8, 2026