Home › China › Philips Goldway (Shenzhen) Industrial Inc.
Manufacturer of medical devices registered in the European database in Shenzhen, China.
| Registration number (SRN) | CN-MF-000003921 |
|---|---|
| Role | Manufacturer |
| Status | Active |
| Country | China |
| City | 518057 Shenzhen |
| Address | Keji North 3rd Road, 2 518057 Shenzhen |
| Registered on | 2021-05-06 |
| FDA establishment register | Registered with the U.S. FDA |
|---|---|
| Matched entry | Philips Goldway (Shenzhen) Industrial Inc. (CN) · FDA 3003687189 |
| Certificate | Status | Expiry | Type | Body |
|---|---|---|---|---|
G15 036155 0072 | valid | 2031-06-03 | Quality management system | NB 0123 |
G10 036155 0060 | valid | expired 2026-08-16 | Quality management system | NB 0123 |
⚠️ State of the register on 2026-08-20. EUDAMED shows only the current version of a certificate — earlier versions are not published, by the Commission or by anyone. A certificate shown as valid here may have changed since. For a legally binding check, consult EUDAMED directly.
The SRN is the registration number assigned by the European Commission. It has been mandatory since 28 May 2026 for any operator placing a medical device on the Union market. Contact details are published in the official register; we do not reproduce them here.
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