FDA device listing
ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE
FDA device listing 1181186516 · Precision Interconnect, LLC
Key facts
| Proprietary names | ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE |
|---|---|
| Owner/operator | Precision Interconnect, LLC |
| Owner/operator number | 9060212 |
| Product codes | LDD |
| Device names | LDD - Dc-Defibrillator, Low-Energy, (Including Paddles) |
| Device class | Class II |
| Classification regulations (21 CFR) | 870.5300 |
| Review panels | Cardiovascular |
| Registered establishments | MAQUILAS TETA KAWI S.A. DE C.V. |
| Establishment registrations | 3003615065 |
| FEI numbers | 3003615065 |
| Establishment operations | Contract 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