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Sign in to claim this brandHenke-Sass, Wolf GmbH
Germany·DE-MF-000005531
Last updated May 24, 2026
What Henke-Sass, Wolf GmbH makes
Henke-Sass, Wolf GmbH manufactures single-use hypodermic needles, general-purpose syringes, metered-delivery hypodermic syringes, insulin syringes with needles, irrigation syringes, ear canal irrigation syringes, and reusable dental anaesthesia syringes. The company also produces rigid optical laparoscopes for minimally invasive surgical procedures.
The devices in the portfolio are classified as Class I and Class II medical devices and are listed in the FDA’s Global Unique Device Identification Database (GUDID). The company is based in Germany.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Henke-Sass, Wolf GmbH manufacture?
Henke-Sass, Wolf GmbH manufactures single-use hypodermic needles, general-purpose syringes, metered-delivery hypodermic syringes, insulin syringes with needles, irrigation syringes, ear canal irrigation syringes, reusable dental anaesthesia syringes, and rigid optical laparoscopes for minimally invasive surgical procedures.
Where is Henke-Sass, Wolf GmbH based?
Henke-Sass, Wolf GmbH is based in Germany, as indicated by the country code DE in the device data.
Which regulatory registries list Henke-Sass, Wolf GmbH's devices?
Henke-Sass, Wolf GmbH's devices are listed in the FDA’s Global Unique Device Identification Database (GUDID), referenced in the data as fda_udi.
How are Henke-Sass, Wolf GmbH's devices classified?
The devices manufactured by Henke-Sass, Wolf GmbH are classified as Class I and Class II medical devices, according to the device classes specified in the data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- Germany
- Address
- 1, Keltenstrasse, Tuttlingen, Germany
- Website
- www.henkesasswolf.de
- —
- —
- [email protected]
- Phone
- 074629466473
- PRRC Contact
- Simon Aichele
- EUDAMED SRN
- DE-MF-000005531
- FDA FEI Number
- —
- DUNS Number
- 317326411
Catalogue (489)
Page 3 of 10| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Lap 5.5/0/300 Hd3 | 8300053462 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4100.000V0 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 22Gx2 3/4-0,70x70 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 4710005016 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 8300014553 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4830003000 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 4710004012 | FDA UDI | Class II | Active |
| Hsw Norm-Ject® | 4020.000V0 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 5102H000V0 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4052D000V0 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 5042H000V0 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 50424000V0 | FDA UDI | Class II | Active |
| Hsw Ligmaject® I | 2101000100 | FDA UDI | Class II | Unknown |
| Hsw Soft-Ject® | 8300005157 | FDA UDI | Class II | Unknown |
| Hsw Soft-Ject® | 5022L000V0 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 8300005762 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 4710011040 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 5100.X00V0 | FDA UDI | Class II | Active |
| Lap 10/0/330 Ak Hd3 | 8300053464 | FDA UDI | Class II | Active |
| Hsw Norm-Ject® | 8300015886 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4710007040 | FDA UDI | Class II | Active |
| Henke-Dent 500 Soft-Grip | 8300042387 | FDA UDI | Class II | Unknown |
| Hsw Fine-Ject® | 4710007050 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 8300015020 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 8300041052 | FDA UDI | Class II | Active |
| Hsw Norm-Ject® | 4030.X90D0 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 8300034773 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 8300033535 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4710004525 | FDA UDI | Class II | Active |
| HSW UNIVERSAL Selffilling ear syringe complete set | 2710036800 | FDA UDI | Class I | Active |
| Hsw Henke-Ject® | 5010.200V0 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 4710018040 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 8300015016 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 5100.000VZ | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 5200.000V0 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4710009050 | FDA UDI | Class II | Active |
| Hsw Fine-Ject | 8300003458 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 5012AA00V0 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 2103000100 | FDA UDI | Class II | Unknown |
| Hsw Norm-Ject® | 4200.000V0 | FDA UDI | Class II | Active |
| Hsw Fine-Ject® | 4710004523 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 8300020995 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4710004512 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 5042G000V0 | FDA UDI | Class II | Active |
| Hsw Norm-Ject® | 4202D000V0 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 8300005761 | FDA UDI | Class II | Active |
| Soft-Ject® | 8300020439 | FDA UDI | Class II | Active |
| Hsw Soft-Ject® | 5202H000V0 | FDA UDI | Class II | Active |
| Hsw Norm-Ject® | 4022B000V0 | FDA UDI | Class II | Active |
| Hsw Henke-Ject® | 4710011040 | FDA UDI | Class II | Active |
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