FDA device listing

Container, Specimen Mailer And Storage, Sterile

FDA device listing 1874789745 · BGS Beta-Gamma-Service GmbH & Co KG

Key facts

Owner/operator BGS Beta-Gamma-Service GmbH & Co KG
Owner/operator number 10043097
Product codes KDT
Device names KDT - Container, Specimen Mailer And Storage, Sterile
Device class Class I
Classification regulations (21 CFR) 864.3250
Review panels Pathology
Registered establishments BGS BETA-GAMMA-SERVICE GMBH & CO KG
Establishment registrations 3009732568
FEI numbers 3009732568
Establishment operations Contract Sterilizer
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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