UDI device identifier
Bruder 98612
UDI device identifier 00041533986126 · The Hilsinger Company Parent, Llc
Key facts
| Primary DI | 00041533986126 |
|---|---|
| Brand name | Bruder |
| Version or model | 98612 |
| Catalog number | 1301852 |
| Company | The Hilsinger Company Parent, Llc |
| DUNS number | 118449190 |
| Product code | HNS |
| GMDN term | Meibomian gland manual expressor/evaluator |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 21, 2025 |
| Version date | Dec 1, 2025 |
| Description | BRUDER RECTANGULAR EXPRESSOR |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: