Trulene
by Healthium Medtech Limited 2 variants
Ref 8G70DZ17DA
Trulene (8G70DZ17DA) is a Class III device made by Healthium Medtech Limited, registered in EUDAMED on 23 Sep 2026 (Basic UDI-DI 8903837H010201010426) with CE/MDR certificate 2022-MDR/QS-011/C valid until 15 Aug 2027, active as of 23 Oct 2026.
Expiring
CE MDR
Valid until
15 Aug 2027
FDA recalls
Not applicable
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8903837H010201010426 08903837820730 | Date23 Sep 2026 | StatusActive |
Official records
- EUDAMED public site 8903837H010201010426
Certificates
- 2022-MDR/QS-011/C Expiring
Quality management system EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 10 Jul 2025
- Expires
- 15 Aug 2027
- Reason
- Other
- 2022-MDR/TD-011/C Expiring
Technical documentation EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 10 Jul 2025
- Expires
- 15 Aug 2027
- Reason
- Other
Timeline
- Certificate issued EUDAMED 2022-MDR/QS-011/C
- Certificate issued EUDAMED 2022-MDR/TD-011/C
- Registered EUDAMED 8903837H010201010426
- Certificate expires EUDAMED 2022-MDR/QS-011/C
- Certificate expires EUDAMED 2022-MDR/TD-011/C
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device name
- Monofilament Polypropylene Sterile Non-Absorbable Surgical Suture
- Model / reference
- 8G70DZ17DA
- Primary DI / UDI-DI
- 08903837820730
- Basic UDI-DI
- 8903837H010201010426
- EMDN code
- H010201010401 Polypropylene monofilament with needle for open surgery
- Device class
- Class III
- EU registration type
- Standard device
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- IN-MF-000008421
- Authorised representative
- Meddevices Lifesciences B.V. NL-AR-000000594
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