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3M COMPANY

United States·US-MF-000014086

Last updated September 17, 2026

Information

Country: United States
Address: 2510, Conway Avenue, St.Paul, United States
Website: solventum.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1(800)634-2249
PRRC Contact: Harry Janiski
EUDAMED SRN: US-MF-000014086
FDA FEI Number: 2110898
DUNS Number: 830016148

Catalogue (3490)

Page 5 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Tegaderm™	90631	FDA UDI	Class I	Active
3M™ Unitek™	900146	FDA UDI	Class I	Active
Ranger™	24500	FDA UDI	Class II	Active
Ketac™	3304P	FDA UDI	Class II	Active
Filtek™	4866C2	FDA UDI	Class II	Active
3M™ Micropore™	1530-12Y	FDA UDI	Class I	Active
Bair Hugger™	55501	FDA UDI	Class II	Active
3M™ Unitek™	900641	FDA UDI	Class I	Active
Filtek™	4864PP	FDA UDI	Class II	Active
3M™ Nexcare™ Stomaseal™	1507	FDA UDI	Class I	Active
3M™ Littmann®	5809	FDA UDI	Class I	Active
Steri-Drape™	9020A	FDA UDI	Class II	Active
Lava™	1314BL-LT	FDA UDI	Class II	Active
3M™ Unitek™	900131	FDA UDI	Class I	Active
3M™ ESPE™ MDI Collared Intermediate O-Ball	2.1 mm x 18 mm	FDA UDI	Class II	Unknown
Vitremer™	3303A3	FDA UDI	Class II	Active
3m™	EXD966-2	FDA UDI	Class II	Active
RelyX™	7614A3	FDA UDI	Class II	Active
Lava™	2012A3-LT	FDA UDI	Class II	Active
Espe™	1942FB	FDA UDI	Class II	Unknown
3m™ Espe™	EUL6	FDA UDI	Class I	Active
3M™ Nexcare™	664-30PB	FDA UDI	Class I	Active
Bair Hugger™	90107	FDA UDI	Class II	Active
3M™ Steri-Drape™	1065B	FDA UDI	Class II	Active
Comply™	1322-12MM	FDA UDI	Class II	Active
Futuro™	71032EN	FDA UDI	Class II	Active
3M™ Unitek™	900347	FDA UDI	Class I	Active
3M™ Unitek™	900520	FDA UDI	Class I	Active
3M™ Unitek™	900523	FDA UDI	Class I	Active
3M™ Steri-Drape™ Cardio/Chest Drape with Ioban™	6682	FDA UDI	Class II	Active
Nova Plus®	V2269T	FDA UDI	Class II	Active
3M™ Attest™	1243RE	FDA UDI	Class II	Active
3m™ Espe™	940531	FDA UDI	Class I	Active
3M™ Filtek™	6550PO	FDA UDI	Class II	Active
3M™ Steri-Strip™	E4542	FDA UDI	Class I	Active
3M™ Unitek™	900436	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5962	FDA UDI	Class I	Active
3M™ Littmann®	2167	FDA UDI	Class I	Active
Filtek™	6028B2E	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2115	FDA UDI	Class I	Active
Lava™	2012A3-HT	FDA UDI	Class II	Active
Lava™	5044A2-HT	FDA UDI	Class II	Unknown
Vitremer™	3303B3	FDA UDI	Class II	Active
3M™ Littmann®	2293	FDA UDI	Class I	Active
3M™ Medipore™	2966	FDA UDI	Class I	Active
3m™	SPS-YP1100	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	U-62	FDA UDI	Class I	Active
3m™ Espe™	940511	FDA UDI	Class I	Active
3M™ Littmann®	6204	FDA UDI	Class I	Active
3M™ Cavilon™	3346	FDA UDI	Class I	Active

Related Companies

Authorised Representatives

3M Deutschland GmbH (Medical) DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (2)

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
Apr 22, 2025	Z-2231-2025	—	open, classified	Notice was issued to clarify flow rates related to the inlet fluid temperature.
Apr 10, 2025	Z-2483-2025	—	open, classified	Field action to clarify the flow rates and inlet fluid temperatures, along with location of the outlet temperature for Ranger Blood/Fluid Warming High Flow Sets.