FDA device listing

Device, Transfer, Patient, Manual

FDA device listing 1901314114 · AMMAR APPAREL II S. DE R.L DE C.V.

Key facts

Owner/operator AMMAR APPAREL II S. DE R.L DE C.V.
Owner/operator number 9057879
Product codes FMR
Device names FMR - Device, Transfer, Patient, Manual
Device class Class I
Classification regulations (21 CFR) 880.6785
Review panels General Hospital
Registered establishments AMMAR APPAREL II S. DE R.L DE C.V.
Establishment registrations 3004133257
FEI numbers 3004133257
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

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