STS Medical Group AD
BG-MF-000041809 · Bulgaria · Sandanski
STS Medical Group AD is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Most frequent device types declared: SECUDRAPE, SECUSORB.
Among these devices, 3 are declared sterile.
Devices declared under this manufacturer
- COMPRESSA OCULARE IN GARZA IDROFILA DI COTONE
- COMPRESSA OCULARE IN TESSUTO NON TESSUTO
- Compressa oculare in garza idrofila di cotone
- Image intensifier drape pack Siemens
- SECUDRAPE
- SECUSORB ABDOMINAL SWABS WITH X-RAY, 45X45 CM, 6 PLIES
- SECUSORB LAPARATOMICHE DI GARZA IDROFILA PURO COTONE TIT 12/8 CON RX,
- SLEEVE PROTECTOR, 20 X 52 CM
- Stool cover
- THORAXCOMPRESS-14PL 70X75/1 STERILE+RIBBONS
Showing 12 of 15 declared devices.
Catalogue references include 03010004, 03010005, 03010006, 500-836, D010021NS, D010022NS.
European nomenclature codes declared: T030199, M040301, T020199, M0201030202, M0201030101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| Country of registration | Bulgaria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 15 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. STS Medical Group AD was not found in either the U.S. or the Canadian register.