Hak
by ChM spółka z ograniczoną odpowiedzialnością 432 variants
Ref 30.1096.000Model RETRACTOR
Active
CE MDR
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number59084472NL111M5 05908447023901 | Date14 Aug 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device name
- Hak
- Model / reference
- RETRACTOR, 30.1096.000
- Primary DI / UDI-DI
- 05908447023901
- Basic UDI-DI
- 59084472NL111M5
- EMDN code
- L03140199 Spreaders and retractors for general surgery, reusable - other
- Device class
- Class I
- EU registration type
- Standard device
- EU market of registration
- Poland
Manufacturer details
- EUDAMED SRN
- PL-MF-000002121
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Properties
Other properties (12)
- Supplied sterile: No
- Implantable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No