FDA device listing
Medline hot/cold packs (disposable),Medline Instant Cold Pack,Medline Instant Hot Pack,Medline Perineal Cold…
FDA device listing 1224701856 · Medline Industries, LP
Key facts
| Proprietary names | Medline hot/cold packs (disposable),Medline Instant Cold Pack,Medline Instant Hot Pack,Medline Perineal Cold Pack,Medline Perineal Warm Pack |
|---|---|
| Owner/operator | Medline Industries, LP |
| Owner/operator number | 1417592 |
| Product codes | IMD |
| Device names | IMD - Pack, Hot Or Cold, Disposable |
| Device class | Class I |
| Classification regulations (21 CFR) | 890.5710 |
| Review panels | Physical Medicine |
| Registered establishments | Medline Industries, LP - Mexicali (MXC), MEDLINE INDUSTRIES, LP - Northfield |
| Establishment registrations | 1417592, 3015173212 |
| FEI numbers | 1417592, 3015173212 |
| Establishment operations | 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