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Hsw Fine-Ject®

FDA UDI

Class II (US FDA UDI)

by Henke-Sass, Wolf GmbH

Identity

Trade Name
HSW FINE-JECT® FDA UDI
Generic Name
Hypodermic needle, single-use FDA UDI
Device Name
HSW FINE-JECT®0,50X40 MM / 25GX1 1/2" STERIL FDA UDI
Model / Reference
8300003551 FDA UDI
Description
HSW FINE-JECT®0,50X40 MM / 25GX1 1/2" STERIL FDA UDI

Identifiers

Catalog Number
8300003551 FDA UDI
Primary DI / UDI-DI
04035873026969 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

Dimensions & Sizes

Size
Length — 40 Millimeter FDA UDI
Outer Diameter — 0.50 Millimeter FDA UDI

Category: Hypodermic needle, single-use

Hsw Fine-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 7041f317-72c8-40c9-a5fa-1ee0edbe0617 36 fields · synced Jun 6, 2026