FDA device listing
MEDLINE / CENTURION STERILE GRAVES VAGINAL SPECULUM,MEDLINE / CENTURION STERILE VAGINAL SPECULUM,Medline / Konig…
FDA device listing 1379586551 · Medline Industries, LP
Key facts
| Proprietary names | MEDLINE / CENTURION STERILE GRAVES VAGINAL SPECULUM,MEDLINE / CENTURION STERILE VAGINAL SPECULUM,Medline / Konig Speculum, Vaginal, Metal,ST.PEDERSON VAGINAL SPECULUM |
|---|---|
| Owner/operator | Medline Industries, LP |
| Owner/operator number | 1417592 |
| Product codes | HDF |
| Device names | HDF - Speculum, Vaginal, Metal |
| Device class | Class I |
| Classification regulations (21 CFR) | 884.4520 |
| Review panels | Obstetrics/Gynecology |
| Registered establishments | Medline Canada, MEDLINE INDUSTRIES, LP - Laredo, Medline Industries, LP - Mexicali (MXC), MEDLINE INDUSTRIES, LP - Northfield, MEDLINE INDUSTRIES, LP (Northpoint Services), Nuevo Laredo Directo al Cliente, PRODUCTOS MEDLINE S.A. DE C.V. |
| Establishment registrations | 1417592, 1422634, 3004122598, 3005595283, 3007289408, 3015173212, 3045816907 |
| FEI numbers | 1417592, 1000514656, 3004122598, 3005595283, 3007289408, 3015173212, 3045816907 |
| Establishment operations | Contract Sterilizer, Foreign Exporter, 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