FDA.reportPublic FDA data

AEROPHARM GmbH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30058318433005831843AEROPHARM GmbH1N2026-01-01Francois-Mitterrand-Allee 1 Rudolstadt Thuringia DE D-07407

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
47622436104100Glatopaject ® - The Glatopaject® is a reusable injection device for the subcutaneous injection of Glatopa®. The Glatopaject® is intended for use with Glatopa® (Glatiramer Acetate Injection) Pre-Filled Syringe.1-800-525-8747qa.druginfo@sandoz.com
57622436104114Glatopaject ® - The Glatopaject® is a reusable injection device for the subcutaneous injection of Glatopa®. The Glatopaject® is intended for use with Glatopa® (Glatiramer Acetate Injection) Pre-Filled Syringe.1-800-525-8747qa.druginfo@sandoz.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3420621472074239K124026LOBSTER AUTO-INJECTORKZH2013-09-13

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KZH12013-09-13

GUDID#