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pfm medical gmbh

Germany·DE-MF-000005190

Last updated September 17, 2026

Information

Country
Germany
Address
60, Wankelstraße, Köln, Germany
Website
www.hico.de/
LinkedIn
—
Facebook
—
Phone
+49221 37678-0
PRRC Contact
Sonia Nexha
EUDAMED SRN
DE-MF-000005190
FDA FEI Number
3003769549
DUNS Number
—

Catalogue (55)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
HICO-Polyurethane-Waterpad SP 550146
EUDAMED
Class IActive
LL 2012/18 Set mit 250 ml Beutel 73018
EUDAMED
Class IIaActive
LL 2012/6 Set m Y-Stück + 2. Leitung 73016
EUDAMED
Class IIaActive
Female drain hose coupling SP 550177
EUDAMED
Class IActive
HICO-Polyurethane-Waterpad 550049
EUDAMED
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (9)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Oct 20, 2014Z-0560-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0565-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0566-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0563-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0564-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0562-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0568-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0561-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

Oct 20, 2014Z-0567-2015—terminated

PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.

FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Pfm Medical, Inc. US