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FDA Import Refusal 799-6827076-1/10002/1 — Euroflex Gmbh

Euroflex Gmbh — FEI 3010097418

The FDA refused shipment 799-6827076-1/10002/1 from Euroflex Gmbh (Germany) on Nov 21, 2025. The refused product falls under Devices — ORTHOPEDIC MANUAL SURGICAL INSTRUMENT. Cited charges: 118,3280

Refusal Details

Date
Nov 21, 2025
Country
Germany
Product Category
Devices
Product Code
87LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Charges
118,3280

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.