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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® 22G X 4 - 0,70 X 100 MM - RW /LB FDA UDI
Model / Reference
22Gx4-0,70x100 FDA UDI
Description
HSW HENKE-JECT® 22G X 4 - 0,70 X 100 MM - RW /LB FDA UDI

Identifiers

Catalog Number
8300059226 FDA UDI
Primary DI / UDI-DI
04035873071136 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

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: Hypodermic needle, single-use

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

Similar devices

Also classified as Hypodermic needle, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0fd6f8e3-64fb-412f-9bf6-f3ad965aea57 35 fields · synced Jun 8, 2026