Hsw Henke-Ject®

FDA UDI

Class II (US FDA UDI)

by Henke-Sass, Wolf GmbH

Identity

Trade Name: HSW HENKE-JECT® FDA UDI
Generic Name: Hypodermic needle, single-use FDA UDI
Device Name: HSW HENKE-JECT® 21G x 2 - 0,80 x 50 MM FDA UDI
Model / Reference: 4710008050 FDA UDI
Description: HSW HENKE-JECT® 21G x 2 - 0,80 x 50 MM FDA UDI

Identifiers

Catalog Number: 4710008050 FDA UDI
Primary DI / UDI-DI: 04035873059080 FDA UDI
FDA Product Code: FMI FDA UDI
GMDN Term: Hypodermic needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5570 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: Length — 50 Millimeter FDA UDI
Outer Diameter — 0.80 Millimeter FDA UDI

Category: Hypodermic needle, single-use

Hsw Henke-Ject® by Henke-Sass, Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Hypodermic needle, single-use.

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EasyTouch — MHC Medical Products · Class II
STERiJECT TM — TSK LABORATORY, JAPAN · Class II
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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: Henke-Sass, Wolf GmbH

Sources (1)

FDA UDI e53246cb-2a67-431c-913d-6094a315a7e3 36 fields · synced Jun 1, 2026