FDA device listing

Pressure Infusion Bag

FDA device listing 1696448872 · Wenzhou Caretek Medical Device Co., Ltd

Key facts

Proprietary names Pressure Infusion Bag
Owner/operator Wenzhou Caretek Medical Device Co., Ltd
Owner/operator number 10029464
Product codes KZD
Device names KZD - Infusor, Pressure, For I.V. Bags
Device class Class I
Classification regulations (21 CFR) 880.5420
Review panels General Hospital
Registered establishments WENZHOU CARETEK MEDICAL DEVICE CO., LTD
Establishment registrations 3007703436
FEI numbers 3007703436
Establishment operations Foreign Exporter
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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