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Baxter Medical Systems GmbH + Co. KG

SAALFELD Thuringia, DE

Baxter Medical Systems GmbH + Co. KG appears in FDA device records in SAALFELD Thuringia, DE. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. As of , FDA records show one recall for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
0
PMA records
0
Recall records
1
Registered establishments
2

FDA records under these names

1 name

FDA records resolved to Baxter Medical Systems GmbH + Co. KG carry these names as well, as FDA wrote them. Each is the firm named on a registration, a 510(k), a PMA, a recall or an enforcement report that was joined to this company on a shared FDA identifier or on a matching name.

  • Kreuzer Gmbh & Co. KGrecall

510(k) clearance history

No 510(k) clearance records for this company in the ingested FDA data.

No 510(k) clearance records in the ingested FDA data.

Registered establishments

FDA registered establishments for Baxter Medical Systems GmbH + Co. KG, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30071432683007143268Baxter Medical Systems GmbH + Co. KGCarl-Zeiss-Str. 7-9, SAALFELD Thuringia 07318 DE2026and 2 more, listed in full below
96814071000182014Baxter Medical Systems GmbH + Co. KGLandsberger Str. 155, Munich Bavaria 80687 DE2026

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-0802-2011klinoPORT, AC powered Operating TableThe motorized adjustable pendant arm may suddenly descend to its lowest position.Terminated

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain