FDA device listing
ACRO Viral Transport Medium,AllTest Viral Transport Medium,Atida Viral Transport Medium,Citest Viral Transport Medium
FDA device listing 1860930704 · Hangzhou AllTest Biotech Co.,Ltd
Key facts
| Proprietary names | ACRO Viral Transport Medium,AllTest Viral Transport Medium,Atida Viral Transport Medium,Citest Viral Transport Medium |
|---|---|
| Owner/operator | Hangzhou AllTest Biotech Co.,Ltd |
| Owner/operator number | 10050156 |
| Premarket submissions | K242576 |
| Product codes | JSM |
| Device names | JSM - Culture Media, Non-Propagating Transport |
| Device class | Class I |
| Classification regulations (21 CFR) | 866.2390 |
| Review panels | Microbiology |
| Registered establishments | Hangzhou AllTest Biotech Co.,Ltd |
| Establishment registrations | 3012073813, 3027519599, 3043127647 |
| FEI numbers | 3012073813, 3027519599, 3043127647 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 100–999 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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