FDA device listing
Cryopres Pro 24 IC, Cryopres Pro 48 SC, Cryopres Pro 24 SC,Deep Freezer: HCLF 225, HCLF 325, HCLF 425, HCLF 525, HCLF…
FDA device listing 1553629467 · Remi Elektrotechnik Ltd.
Key facts
| Proprietary names | Cryopres Pro 24 IC, Cryopres Pro 48 SC, Cryopres Pro 24 SC,Deep Freezer : HCLF 225, HCLF 325, HCLF 425, HCLF 525, HCLF 625, HCLF 225 Ultra, HCLF 325 Ultra, HCLF 425 Ultra,Deep freezer RQV200 Plus, RQV300 Plus, RQV400 Plus, RQV500 Plus, RQV600 Plus RQVD200 Plus, RQVD300 Plus, RQVD400 Plus,Deep Freezer: RQV 600i Plus,Deep freezer: Sero Freeze 245, Sero Freeze 340, MBT 100,HCLF 525 Ultra, HCLF 625… |
|---|---|
| Owner/operator | Remi Elektrotechnik Ltd. |
| Owner/operator number | 10050790 |
| Product codes | JRM |
| Device names | JRM - Freezer |
| Device class | Class I |
| Classification regulations (21 CFR) | 862.2050 |
| Review panels | Clinical Chemistry |
| Registered establishments | Remi Elektrotechnik Ltd. |
| Establishment registrations | 3012315023 |
| FEI numbers | 3012315023 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database