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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: —
Email: [email protected]
Phone: +49221 37678-0
PRRC Contact: Sonia Nexha
EUDAMED SRN: DE-MF-000005190
FDA FEI Number: 3003769549
DUNS Number: —

Catalogue (55)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
Multi-Snare	147315	FDA UDI	Class II	Active
Multi-Snare	147305	EUDAMEDFDA UDI	Class II	Active
Mulit-Snare	147302	FDA UDI	Class II	Active
HICO-Water drain hose	550076	EUDAMED	Class I	Active
HICO-Polyurethane-Waterpad	550026	EUDAMED	Class I	Active
Female drain hose coupling	550077	EUDAMED	Class I	Active
LL 2012/24 Set mit 0, 2 Filter	73024	EUDAMED	Class IIa	Active
Clamp holder	592900	EUDAMED	Class I	Active
HICO-Variotherm 555	600021	EUDAMED	Class IIb	Active
APL2002/24 Set mit 0, 2 Filter	52024	EUDAMED	Class IIa	Active
APL2002/3 Set mit 150 ml Reservoir	52013	EUDAMED	Class IIa	Active
HICO-Hose extension thermo insulated	600022	EUDAMED	Class I	Active
APL2002/6 Set m Y-Stück + 2. Leitung	52016	EUDAMED	Class IIa	Active
HICO-Hose extension SP thermo insulated	600090	EUDAMED	Class I	Active
HICO-Hose extension SP	550090	EUDAMED	Class I	Active
LL 2012/2 Set mit Anstechdorn u. 1, 2 Fi	73012	EUDAMED	Class IIa	Active
LL 2012/34 Set Spiral, Y w Luer+RV, 0, 2	73034	EUDAMED	Class IIa	Active
Equipotential bonding cable 1m	592905	EUDAMED	Class I	Active
Male drain hose coupling	550078	EUDAMED	Class I	Active
HICO-Aquatherm 660	590001	EUDAMED	Class IIb	Active
HICO-Polyurethane-Waterpad	550047	EUDAMED	Class I	Active
APL2002/4 Set m. 150 ml Res. u. 0, 2 Filt	52014	EUDAMED	Class IIa	Active
LL 2012/41 Set mit UV-Lichtschutz	73041	EUDAMED	Class IIa	Active
LL 2012/1 Set mit Anstechdorn	73011	EUDAMED	Class IIa	Active
LL 2012/22 Set mit Luer	73022	EUDAMED	Class IIa	Active
APL2002/34 Set Spiral, Y w Luer+RV, 0, 2	52034	EUDAMED	Class IIa	Active
LL 2012/3 mit 150 ml Reservoir	73013	EUDAMED	Class IIa	Active
HICO-Aquatherm 660	590020	EUDAMED	Class IIb	Active
LL 2012/25 Set Spiral, Y w Luer+RV, 1, 2	73025	EUDAMED	Class IIa	Active
HICO-Polyurethane-Waterpad SP	550144	EUDAMED	Class I	Active
APL2002/1 Set mit Anstechdorn	52011	EUDAMED	Class IIa	Active
APL2002/9 Set mit Anstechdorn u. 1, 2 Fil	52019	EUDAMED	Class IIa	Active
LL 2012/26 Set Spirale und 1, 2 Filter	73026	EUDAMED	Class IIa	Active
Male drain hose coupling SP	550178	EUDAMED	Class I	Active
APL2002/22 Set mit Luer und 1, 2 Filter	52022	EUDAMED	Class IIa	Active
APL2002/26 Set Spirale und 1, 2 Filter	52026	EUDAMED	Class IIa	Active
APL2002/5 Set m gelber Leitung + 0, 2 Fil	52015	EUDAMED	Class IIa	Active
LL 2012/5 Set m gelber Leitung + 0, 2 Fil	73015	EUDAMED	Class IIa	Active
LL 2012/4 Set m. 150 ml Res. u. 0, 2 Fil	73014	EUDAMED	Class IIa	Active
LL 2012/9 Set mit Anstechdorn u. 1, 2 Fi	73019	EUDAMED	Class IIa	Active
APL2002/25 Set Spiral, Y w Luer+RV, 1, 2	52025	EUDAMED	Class IIa	Active
Stand plate complete	542810	EUDAMED	Class I	Active
pfm NeoBreathe CPAP Ventil	NEONB	EUDAMED	Class I	Active
Redon-Connector	20818	EUDAMED	Class I	Active
LL 2012/27 Set mit Tropfkammer	73027	EUDAMED	Class IIa	Active
HICO-Variotherm 555	600001	EUDAMED	Class IIb	Active
HICO-Variotherm 550	540021	EUDAMED	Class IIb	Active
APL2002/2 Set mit Anstechdorn u. 1, 2 Fil	52012	EUDAMED	Class IIa	Active
HICO-Polyurethane-Waterpad SP	550147	EUDAMED	Class I	Active
HICO-Hose extension (disposable pads)	550069	EUDAMED	Class I	Active

Related Companies

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Authorities

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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.

Date	Recall No.	Class	Status	Reason
Oct 20, 2014	Z-0560-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0565-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0566-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0563-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0564-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0562-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0568-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-0561-2015	—	terminated	PFM Medical is recalling catheters and other medical devices because they may exceed USP limits for bacterial endotoxin.
Oct 20, 2014	Z-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