Stihler Electronic GmbH
Stihler Electronic GmbH holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2026, with 3 FDA device recalls on record.
Top product codes for Stihler Electronic GmbH
FDA recalls by Stihler Electronic GmbH
- Z-0759-2019 — Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Product Code: PF2-WP33 Product Usage: The PRISMAFLO IIS warmer is used for warming return blood flow.
- Z-0760-2019 — Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Product Code: PF2-WP31 Product Usage: The PRISMAFLO IIS warmer is used for warming return blood flow.
- Z-0761-2019 — Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product Code: PF2-WP2618 Product Usage: The PRISMAFLO IIS warmer is used for warming return blood flow.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Stihler Electronic GmbH
Data sourced from openFDA. This site is unofficial and independent of the FDA.