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Hsw Soft-Ject®

FDA UDI

Class II (US FDA UDI)

by Henke-Sass, Wolf GmbH

Identity

Trade Name
HSW SOFT-JECT® FDA UDI
Generic Name
Insulin syringe/needle, basic FDA UDI
Device Name
1 ML HSW SOFT-JECT® INS 100IU BK 0,50X16/25GX5/8 FDA UDI
Model / Reference
5012BA00V0 FDA UDI
Description
1 ML HSW SOFT-JECT® INS 100IU BK 0,50X16/25GX5/8 FDA UDI

Identifiers

Catalog Number
5012BA00V0 FDA UDI
Primary DI / UDI-DI
04035873019565 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Insulin syringe/needle, basic 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

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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
Total Volume — 1 Milliliter FDA UDI

Category: Insulin syringe/needle, basic

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

Similar devices

Also classified as Insulin syringe/needle, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 79fb46a5-79aa-4743-b524-4c2c9df6476d 36 fields · synced Jun 8, 2026