FDA device listing
DYNACOR SUCTION CONNECTING TUBING,Lingeman,Medline 5-in-1 connector,Medline Connecting Tubing,MEDLINE TUBE, ASPIRATING…
FDA device listing 1521583301 · Medline Industries, LP
Key facts
| Proprietary names | DYNACOR SUCTION CONNECTING TUBING,Lingeman,Medline 5-in-1 connector,Medline Connecting Tubing,MEDLINE TUBE, ASPIRATING, FLEXIBLE, CONNECTING - BYY |
|---|---|
| Owner/operator | Medline Industries, LP |
| Owner/operator number | 1417592 |
| Product codes | BYY |
| Device names | BYY - Tube, Aspirating, Flexible, Connecting |
| Device class | Class II |
| Classification regulations (21 CFR) | 880.6740 |
| Review panels | General Hospital |
| Registered establishments | Medline Industries, LP - Mexicali (MXC), MEDLINE INDUSTRIES, LP - Northfield, MEDLINE INDUSTRIES, LP (Northpoint Services), MICROTEK DOMINICANA, S.A.S., Microtek Medical LLC |
| Establishment registrations | 1417592, 1422634, 8043817, 3015173212, 3021970868 |
| FEI numbers | 1417592, 1000514656, 3003094575, 3015173212, 3021970868 |
| Establishment operations | Contract Sterilizer, Repackager/Relabeler, Specification Developer |
| 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