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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 2 of 10

Device	Model / Reference	Registries	Class	Status
Wells	WELL-2318501	EUDAMED	Class IIa	Active
Care PLUS	THG-38207 /76-38207 / 202401	EUDAMED	Class IIa	Active
Mercurochrome	JUV-050124 / F050124C	EUDAMED	Class IIa	Active
Dr. Scholl's	SCH-9038278 / 76-9038278-0125	EUDAMED	Class IIa	Active
Medipeed	UN-SD540035	EUDAMED	Class IIa	Active
ProFoot	PRO-71617	EUDAMED	Class IIa	Active
Podia	NP-0001	EUDAMED	Class IIa	Active
matas STRIBER	MAT-CP1000 / CP-1000	EUDAMED	Class IIa	Active
Heka	VH-OT0170-2	EUDAMED	Class IIa	Active
Dr. Scholl's	SCH-9038276 / 76-9038276	EUDAMED	Class IIa	Active
Medipeed	UN-SD540025	EUDAMED	Class IIa	Active
Mercurochrome	JUV-050119 / F050119C	EUDAMED	Class IIa	Active
Steripan	LBD-312040 9 / 312040v9	EUDAMED	Class IIa	Active
Gilbert	GIL-251574	EUDAMED	Class IIa	Active
Hershey's S'mores	017276237986	FDA UDI	Class I	Unknown
Hot Wheels	017276239911	FDA UDI	Class I	Active
Batman Adhesive Bandages	017276236866	FDA UDI	Class I	Active
Sesame Street -Furry Friends Forever	017276238518	FDA UDI	Class I	Active
My Little Pony	017276238259	FDA UDI	Class I	Active
Care Science	017276238501	FDA UDI	Class I	Active
Aquaman	017276238884	FDA UDI	Class I	Unknown
Care Band Adhesive Bandages	CBD4019	FDA UDI	Class I	Active
ALL-HEALTH Wound Care Products	017276234466	FDA UDI	N	Active
The Elf on the Shelf	017276235708	FDA UDI	Class I	Unknown
CarePak	017276237658	FDA UDI	Class I	Active
Wonder Woman	017276237955	FDA UDI	Class I	Active
ALL-HEALTH Adhesive Bandages	017276234121	FDA UDI	Class I	Active
Care Band Adhesive Bandages	CBD2018	FDA UDI	Class I	Active
CarePak	017276229431	FDA UDI	Class I	Active
Jojo Siwa	017276237146	FDA UDI	Class I	Unknown
My little pony	017276238266	FDA UDI	Class I	Active
ALL-HEALTH Hydrocolloid Gel Cushions	017276233957	FDA UDI	Class I	Unknown
Sesame Street	017276238372	FDA UDI	Class I	Unknown
Care Science	017276234176	FDA UDI	N	Unknown
My Little Pony	017276232394	FDA UDI	Class I	Unknown
Care Band Adhesive Bandages	CBD4016	FDA UDI	Class I	Active
DC Super Friends	017276238808	FDA UDI	Class I	Unknown
Dreamworks Gabby's Dollhouse	017276238648	FDA UDI	Class I	Unknown
Rapid Seal	00017276239423	FDA UDI	U	Active
CarePak	017276238075	FDA UDI	Class I	Active
CarePak	017276229158	FDA UDI	Class I	Active
Clear Passage Nasal Strips	017276234190	FDA UDI	Class I	Active
Hatchimals	017276234565	FDA UDI	Class I	Active
Scoob!	017276237849	FDA UDI	Class I	Active
Jurassic World Camp Cretaceous	017276238945	FDA UDI	Class I	Active
Sesame Street	017276233216	FDA UDI	Class I	Active
Tech Deck	017276237979	FDA UDI	Class I	Active
JOJO Siwa	017276237283	FDA UDI	Class I	Unknown
Wonder Woman	017276237825	FDA UDI	Class I	Active
Llama	017276237252	FDA UDI	Class I	Unknown

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.