Laboratoire Huckert's EUDAMED Devices and Notified Body
Researched with the BEUDAMED Research Assistant on July 11, 2026. Answers are generated from the BEUDAMED database and cite their records — verify time-critical facts against official sources.
Laboratoire Huckert’s International (SRN BE-MF-000024078) has 25 on-market EUDAMED device records. The records are primarily MDD Class IIa/IIb, with one MDR Class IIa listing. The registered products are:
| Product family / device | Registered presentations |
|---|---|
| UMONIUM38® Sterily | 125 ml, 1 L, 5 L (listed as “UMONIU38®”) |
| UMONIUM38® Neutralis | 125 ml, 5 L, general entry |
| UMONIUM38® Neutralis Spray | 250 ml, 500 ml |
| UMONIUM38® Instruments | 125 ml, 1 L, 5 L |
| UMONIUM38® Equipments | 125 ml, 1 L, 5 L |
| UMONIUM38® Medical Spray | 250 ml, 1 L |
| UMONIUM38® Probes | 1 piece, 100 pieces, 2 × 50 pieces |
| UMONIUM38® Medical Tissues | 1 piece, 95 pieces, 100 pieces |
| UMONIUM38® Neutralis Tissues | 1 piece, 100 pieces |
| Labocid | UMONIMU38® Labocid |
Notified body: the certificates associated with these registrations name SGS Belgium NV, notified body 1639, as the certifying body. The certificates are MDD Annex II (excluding Section 4): BE19819943486 (also represented by a duplicate-format record) and BE19/819943486, each showing an expiry date of 2028-12-31. The dataset does not map a current certificate status, so this should be confirmed against the official EUDAMED source for time-critical use.
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