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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 16 of 70

Device	Model / Reference	Registries	Class	Status
Littmann®	3100BK27	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6202	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5631	FDA UDI	Class I	Active
Lava™	5074B1-HT	FDA UDI	Class II	Active
3m™	9160	FDA UDI	Class II	Active
Futuro™	71071EN	FDA UDI	Class II	Active
3m™	1840FS	FDA UDI	Class II	Active
3M™ Nexcare™ Active™	516-30PB	FDA UDI	Class I	Active
3M™ Micropore™	1530S-1	FDA UDI	Class I	Active
Bair Hugger™	58501	FDA UDI	Class II	Active
3M™ Steri-Strip™	R1546	FDA UDI	Class I	Active
3m™ Espe™	6UL2	FDA UDI	Class I	Active
3M™ Transpore™	1527-636	FDA UDI	Class I	Active
Ranger™	24110	FDA UDI	Class II	Active
3M™ Nexcare™ Steri-Strip™	H1547	FDA UDI	Class I	Active
3M™ Tegaderm™	90022	FDA UDI	Class I	Active
3M™ Ranger™	14500	FDA UDI	Class I	Active
Bair Hugger™	57000	FDA UDI	Class II	Active
Steri-Vac™	GS8-1D	FDA UDI	Class II	Active
3m™ Espe™	940435	FDA UDI	Class I	Active
Tegaderm™	77-2100K01	FDA UDI	U	Active
Filtek™	6028WE	FDA UDI	Class II	Active
3M™ Cavilon™	3343N	FDA UDI	Class I	Active
Ranger™	29500	FDA UDI	Class II	Active
3m™ Espe™	ELL2	FDA UDI	Class I	Active
Comply™	1355-24MM	FDA UDI	Class II	Active
Steri-Drape™	1081P	FDA UDI	Class II	Active
3M™ Nexcare™	AWP-34	FDA UDI	Class I	Active
3M™ Tegaderm™	9132	FDA UDI	U	Active
3M™ Attest™	1348E	FDA UDI	Class II	Active
3m™ Espe™	940513	FDA UDI	Class I	Active
3M™ Unitek™	900124	FDA UDI	Class I	Active
3m™ Espe™	1919	FDA UDI	Class I	Active
Ranger™	24365	FDA UDI	Class II	Unknown
3M™ Micropore™	1530S-1	FDA UDI	Class I	Active
Nova Plus®	9160V	FDA UDI	Class II	Unknown
3M™ Littmann® Classic III™	5806	FDA UDI	Class I	Active
3M™ Cavilon™	3342K	FDA UDI	Class I	Active
3m™ Espe™	DUR5	FDA UDI	Class I	Active
3M™ Unitek™	900516	FDA UDI	Class I	Active
3M™ Littmann®	5831	FDA UDI	Class I	Active
3M™ Littmann® Master Cardiology™	2165	FDA UDI	Class I	Active
3M™ Nexcare™	H3564	FDA UDI	Class I	Active
Bair Hugger™	81001	FDA UDI	Class II	Active
3M™ Precise™	SR-3	FDA UDI	Class I	Active
Filtek™	6033A2	FDA UDI	Class II	Active
Bair Hugger™ Novaplus™	45534	FDA UDI	Class II	Active
3M™ Micropore™	1532-1	FDA UDI	Class I	Active
3M™ Ioban™	8851EZ	FDA UDI	Class II	Active
3M™ Littmann®	2114	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.