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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
Irrigation syringe FDA UDI
Device Name
HSW HENKE-JECT® 3-TLG. 100 ML (120 ML) CATHETER FDA UDI
Model / Reference
8300005458 FDA UDI
Description
HSW HENKE-JECT® 3-TLG. 100 ML (120 ML) CATHETER FDA UDI

Identifiers

Catalog Number
8300005458 FDA UDI
Primary DI / UDI-DI
04035873060017 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Irrigation syringe 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

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
Total Volume — 100 Milliliter FDA UDI

Category: Irrigation syringe

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 Irrigation syringe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e1fee332-ca1c-41bf-8cc7-b0d0f5613066 36 fields · synced May 30, 2026