Certificates of Conformity
Medical Devices by ТОВ "ММ МЕДІК"
ТОВ "ММ МЕДІК" manufactures and sells medical devices in compliance with the requirements of the current legislation of Ukraine. All products listed on the website mm-medic.com have undergone the conformity assessment procedure in accordance with the Technical Regulation on Medical Devices, approved by Resolution No. 753 of the Cabinet of Ministers of Ukraine dated October 2, 2013.
1. Certificate of Conformity for Medical Devices
| Certificate number | UA.101.MD.3.0444-24.00 |
| Registration date | 04.12.2025 |
| Valid until | 13.01.2029 |
| Conformity assessment body | ДУО "ПОЛІТЕХМЕД" (UA.TR. 101) |
| Manufacturer | ТОВ «ММ МЕДИК» |
Products covered by the certificate:
- Plasmotherapy tubes
- Fibrin collection tubes
- PRP tubes
- Vacuum tube needles
- Disposable sterile injection syringes
- Butterfly catheters for vacuum tubes
- Disposable sterile blood collection needles
2. Quality Management System Certificate (ISO 13485:2016)
| Certificate number | UA.101.QMS.-23.00 |
| Standard | ISO 13485:2016 |
| Registration date | 18.08.2023 |
| Valid until | 17.08.2026 |
| Conformity assessment body | ДУО "ПОЛІТЕХМЕД" (UA.TR. 101) |
Scope of certification:
Design, development, manufacture, and sale of medical devices (vacuum blood collection systems, in vitro diagnostic laboratory devices).
3. Verification of Certificate Validity
The validity of the certificates listed above can be verified in the official Registry of the Designated Conformity Assessment Body ДУО "ПОЛІТЕХМЕД" at: politekhmed.ua.
4. Obtaining Copies of Certificates
To obtain certified copies of certificates of conformity or additional information regarding product certification, please contact:
Copies of certificates are provided upon request within 3 business days.