Establishment registration
PULSION MEDICAL SYSTEMS SE
FDA establishment registration 3003263092 · Aschheim, DE
Key facts
| Registration number | 3003263092 |
|---|---|
| Establishment name | PULSION MEDICAL SYSTEMS SE |
| Owner/operator | Maquet Critical Care AB |
| Owner/operator number | 9036213 |
| FEI number | 3003263092 |
| Address | Einstein Ring 30 |
| City | Aschheim |
| Country | DE |
| Registration valid through | 2026 |
| Product codes listed | BZC, BZQ, CBQ, CBR, CBS, CCK, CCL, DPS, DQA, DRG, DRJ, DRQ, DRS, DRT, DRW, DSA, DSF, DSH, DSI, DSJ, DSK, DSP, DXG, DXN, FLL, GWS, KLK, KOI, KRB, KRC and 9 more |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database