Atlas Medical GmbH
DE-MF-000029961 · Germany · Blankenfelde-Mahlow OT Dahlewitz
Atlas Medical GmbH is registered in the European database on medical devices as a manufacturer, with 179 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
Most frequent device types declared: 70023001, 8.00.17.0.0025, 8.01.00.0.0005, 8.01.00.0.0050, 8.01.07.0.0005.
Among these devices, 1 are declared sterile.
Devices declared under this manufacturer
- ABO Set (Anti-A (1/256), Anti-B (1/256), Anti-D (1/64)), 3x10ml/ Plast
- Anti-A Monoclonal Reagent (Titer: 1/256), 10ml/vial, 10 vials/Plastic
- Atlas
- Atlas Activated Partial Thromboplastin Time (APTT) Reagent, 2x2 ml APT
- Atlas Bovine Albumin 30%, 10 ml/Vial, 10 vials/Pack.
- Atlas Brucella Rose Bengal Kit , 50 Tests
- Atlas Brucella Rose Bengal Reagent, 5ml/vial
- Atlas D-Dimer Latex Kit, 25 Tests
- Atlas Febrile Antigen Set (10 Antigens: Salmonella OA, OB, OC, OD, HA,
- Atlas Home Liver Function Test
- Atlas Proteus OX2 Reagent, 5 ml/vial, 1 vial/Box.
- Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slid
Showing 12 of 179 declared devices.
Catalogue references include 8.00.17.0.0025, 8.01.00.0.0005, 8.01.00.0.0050, 8.01.07.0.0005, 8.01.12.0.0005, 8.01.17.0.0050.
European nomenclature codes declared: W0105011003, W0103030199, W0101060204, W0105010399, W0105011701, W01021110.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ATLAS MEDICAL (JO) · FDA 3007126977 |
| Devices in EUDAMED | 179 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 179 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | ATLAS MEDIC INC. |
⚠️ A similar name exists; unverified — why.
What it holds in Canada
| Licences on record | 24 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 24 |
| First licensed | 2019-11-05 |
Licence types: System (15), Single Device (6), Device Group Family (2), Device Family (1).
Licensed under: MEDUP TENS (TRANSCUTANEOUS NERVE STIMULATOR), MEDUP V3 ACTIVE PASSIVE TRAINER FOR UPPER AND , MEDUP EMS (ELECTRICAL MUSCLE STIMULATOR), MEDUP PX20 COMPRESSION THERAPY DEVICE, ACUPUNCTURE DRY NEEDLES, SHOCKPULSAR SX20 EXTRACORPOREAL SHOCK WAVE THE.