Is this your brand? Sign in to claim ownership.

Aso LLC

United States·US-MF-000008641

Last updated September 17, 2026

Information

Country: United States
Address: 300, Sarasota Center Blvd., Sarasota, United States
Website: www.asoeurope.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +31 24 343 54 80
PRRC Contact: Federico Juliao
EUDAMED SRN: US-MF-000008641
FDA FEI Number: 1038758
DUNS Number: 152793493

Catalogue (478)

Page 10 of 10

Device	Model / Reference	Registries	Class	Status
Boni	BON-282278	EUDAMED	Class IIa	Active
Solupharm	SOL-COS140	EUDAMED	Class IIa	Active
Senti2	SEN-FOT002	EUDAMED	Class IIa	Active
Mivolis	MIV-081114	EUDAMED	Class I	Active
Heka	VH-OT0172	EUDAMED	Class IIa	Active
Zzzquil	ZQ-80814519	EUDAMED	Class I	Active
Care Plus	THG-38208	EUDAMED	Class IIa	Active
Prontex	SAF-16809	EUDAMED	Class IIa	Active
Medicare	FLM-MD187 V.6 ECO	EUDAMED	Class IIa	Active
Urgo	UR-604629	EUDAMED	Class IIa	Active
Deramed	FRE-00059 / F-0059-01C	EUDAMED	Class IIa	Active
Botikit	BOT-FOT008	EUDAMED	Class IIa	Active
Flowplast	FLP-082023	EUDAMED	Class I	Active
Silavit	Silavit	EUDAMED	Class I	Active
M-Classic	BEV-7221	EUDAMED	Class I	Active
Gehwol	GE-102762001	EUDAMED	Class IIa	Active
Medicare	FLM-MD189 V.6 ECO	EUDAMED	Class IIa	Active
Medicare	FLM-MD197 V.6 ECO	EUDAMED	Class IIa	Active
Apoteket	AT-215307	EUDAMED	Class IIa	Active
Urgo	UR-604138	EUDAMED	Class IIa	Active
Senti2	SEN-FOT001	EUDAMED	Class IIa	Active
Apotek	APO-52702	EUDAMED	Class IIa	Active
ZzzzQuil	ZQ-80814523	EUDAMED	Class I	Active
Etos	ET-521850043	EUDAMED	Class IIa	Active
Airmax	AIR-7611	EUDAMED	Class I	Active
Albert Heijn	AH-181850016	EUDAMED	Class IIa	Active
Flexipro	NOR-FOT010	EUDAMED	Class IIa	Active
Clarel Adbene	CLA-FOT004	EUDAMED	Class IIa	Active

Related Companies

Authorised Representatives

Aso Europe BV NL

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (15)

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
Mar 23, 2023	Z-1499-2023	—	open, classified	The adhesive bandage contains 0.1% benzalkonium chloride impregnated in the pad and is not disclosed on the labeling.
Jun 22, 2022	Z-1517-2022	—	open, classified	The product falls apart during handling after removal from its primary packaging.
Mar 2, 2022	Z-1031-2022	—	terminated	Kits contained recalled acetaminophen.
Oct 16, 2018	Z-0525-2019	—	open, classified	Potential that gauze pads may not be fully sterilized
Jun 10, 2015	Z-2460-2015	—	terminated	Contain 0.1% Benzalkonium Chloride in the 5/8 bandages inside the assortment which is not listed as an active ingredient in the product label.
Aug 21, 2013	Z-0004-2014	—	terminated	No antibacterial bandages were packed in boxes labeled as antibacterial.
Jul 26, 2013	Z-1890-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1892-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1891-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1894-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1893-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1895-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1896-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1889-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.
Jul 26, 2013	Z-1888-2013	—	terminated	This recall has been initiated by Aspen Surgical Products, Inc., due to the inability to confirm sterility.