# MEDI.PLAN GMBH & CO. KG

FEI: 3033536319
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: MEDI.PLAN GmbH & Co. KG (#10091549)

Address: Hofkerstrabe 22, Dortmund North Rhine-Westphalia, 44149, DE

Mandatory US Agent: Capote Law Firm

## Products

Total registered: 1
Top product codes: FMI
Regulation §: 880.5570

Proprietary names: BD SAFETYGLIDE NEEDLE 25GX1" PACK 50, BD SAFETYGLIDE NEEDLE 21GX1" PACK 50, BD SAFETYGLIDE NEEDLE 23GX1" PACK 50, BD SAFETYGLIDE NEEDLE 25GX1-1/2 PACK 50, BD SAFETYGLIDE NEEDLE 25GX5/8" PACK 50, BD SAFETYGLIDE NEEDLE 18GX1-1/2 PACK 50

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223033536319%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3033536319