FDA device listing
ALKALINE PHOSPHATASE,AMYL-P 600Tests cobas c701,AMY-P, 200Tests, cobas c, Integra,cobas c 70X…
FDA device listing 1102660125 · Roche Diagnostics Operations Inc.
Key facts
| Proprietary names | ALKALINE PHOSPHATASE,AMYL-P 600Tests cobas c701,AMY-P, 200Tests, cobas c, Integra,cobas c 70X Amylase-pancreatic/600,Pancreas a - Amylase 100 c111,Pankreas a - Amylase 100 c111 |
|---|---|
| Owner/operator | Roche Diagnostics Operations Inc. |
| Owner/operator number | 9039767 |
| Premarket submissions | K981897 |
| Product codes | CJE, DCK, JFJ |
| Device names | CJE - Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes, DCK - C-Reactive Protein, Antigen, Antiserum, And Control, JFJ - Catalytic Methods, Amylase |
| Device class | Class II |
| Classification regulations (21 CFR) | 862.1050, 862.1070, 866.5270 |
| Review panels | Clinical Chemistry, Immunology |
| Registered establishments | ROCHE DIAGNOSTICS GMBH |
| Establishment registrations | 9610126 |
| FEI numbers | 3002806559 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 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