Skip to the page

Data / Medical devices / Container, Specimen Mailer And Storage, Non-Sterile / Germany

FDA-registered makers of Container, Specimen Mailer And Storage, Non-Sterile in Germany: 7 establishments

7 establishments in Germany are registered with the FDA to make Container, Specimen Mailer And Storage, Non-Sterile (product code NNK). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Device
Container, Specimen Mailer And Storage, Non-Sterile
Product code
NNK
Country
Germany

Makers of Container, Specimen Mailer And Storage, Non-Sterile in Germany

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ahlstrom Germany GMBHBarenstein Saxony, GermanyManufacturer0000api.fda.gov
DRG Instruments GMBHMARBURG Hesse, GermanyComplaint file establishment, Manufacturer0000api.fda.gov
Immundiagnostik AGBensheim Hesse, GermanyManufacturer0000api.fda.gov
Med Auxil Analysis Aids E.K.Seesen Lower Saxony, GermanyManufacturer0000api.fda.gov
Medite Medical GMBHBurgdorf Lower Saxony, GermanyManufacturer0000api.fda.gov
Sarstedt AG & Co. KGNUMBRECHT North Rhine-Westphalia, GermanyManufacturer0000api.fda.gov
Schebo Biotech AGGIESSEN Hesse, GermanyForeign private label distributor, Manufacturer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.