Solus
by TI Medical Private Limited 186 variants
Ref TI/C-BRO/01Model Braided Coated Polyglycolic acid suture with needle (Violet)
Active
CE MDR
Valid until
22 Mar 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number89042482SOL001PE | Date24 Mar 2026 | StatusActive |
Certificates
- 2975-MED-2608201 Active
Quality management system EU MDR
- Certifier
- SZUTEST Konformitätsbewertungsstelle GmbH 2975
- Issued
- 23 Mar 2026
- Expires
- 22 Mar 2031
- 2975-MED-2608201-D01 Active
Technical documentation EU MDR
- Certifier
- SZUTEST Konformitätsbewertungsstelle GmbH 2975
- Issued
- 23 Mar 2026
- Expires
- 22 Mar 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
EU market availability
Made available in 32 countries, as listed in EUDAMED:
- Austria since 9 Jun 2016
- Belgium since 9 Jun 2016
- Bulgaria since 9 Jun 2016
- Croatia since 9 Jun 2016
- Cyprus since 9 Jun 2016
- Czechia since 9 Jun 2016
- Denmark since 9 Jun 2016
- Estonia since 9 Jun 2016
- Finland since 9 Jun 2016
- France since 9 Jun 2016
- Germany since 9 Jun 2016
- Greece since 9 Jun 2016
- Hungary since 9 Jun 2016
- Iceland since 9 Jun 2016
- Ireland since 9 Jun 2016
- Italy since 9 Jun 2016
- Latvia since 9 Jun 2016
- Liechtenstein since 9 Jun 2016
- Lithuania since 9 Jun 2016
- Luxembourg since 9 Jun 2016
- Malta since 9 Jun 2016
- Netherlands since 9 Jun 2016
- Northern Ireland since 9 Jun 2016
- Norway since 9 Jun 2016
- Poland since 9 Jun 2016
- Portugal since 9 Jun 2016
- Romania since 9 Jun 2016
- Slovakia since 9 Jun 2016
- Slovenia since 9 Jun 2016
- Spain since 9 Jun 2016
- Sweden since 9 Jun 2016
- Türkiye since 9 Jun 2016
Specification
- Device Name
- Braided Coated Polyglycolic acid suture
- Model / Reference
- Braided Coated Polyglycolic acid suture with needle (Violet), TI/C-BRO/01
- Primary DI / UDI-DI
- 08904248264267, 08904248264359, 08904248200975, 08904248276925, 08904248201019, 08904248284937, 08904248201408, 08904248261235, 08904248200579, 08904248266261, 08904248200418, 08904248257245, 08904248277632, 08904248276871, 08904248261372, 08904248200678, 08904248274259, 08904248264335, 08904248296176, 08904248267831, 08904248200807, 08904248248496, 08904248279520, 08904248261440, 08909296023804, 08904248200661, 08904248200562, 08904248240001, 08904248267626, 08904248231948, 08904248275485, 08904248233119, 08904248284920, 08904248275638, 08904248288737, 08904248200401, 08904248287433, 08909296017520, 08904248264311, 08904248201149, 08904248246577, 08904248264472, 08909296015878, 08904248287488, 08904248266292, 08904248201187, 08909296004827, 08904248201231, 08904248284715, 08904248279391
- Basic UDI-DI
- 89042482SOL001PE
- EMDN Code
- H010101020101, H010101020103
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- IN-MF-000026561
- Authorised representative
- Obelis s.a. BE-AR-000000106
Other devices from TI Medical Private Limited
Properties
Other properties (11)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No