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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 15 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Medipore™	3566	FDA UDI	Class I	Active
Red Dot™	2259-50	FDA UDI	Class II	Active
3M™ Nexcare™	SSB-20A	FDA UDI	Class I	Active
Filtek™	6033A1	FDA UDI	Class II	Active
3m™ Espe™	940326	FDA UDI	Class I	Active
Vitremer™	3303PEDO	FDA UDI	Class II	Active
3M™ ESPE™ Protemp™	50614	FDA UDI	Class I	Active
3M™ Steri-Strip™	E4548	FDA UDI	Class I	Active
Comply™	1322-48MM	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-41	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	L-68	FDA UDI	Class I	Active
Futuro™	71036BLEN	FDA UDI	Class II	Active
Bair Hugger™	42568	FDA UDI	Class II	Active
Filtek™	6029A2D	FDA UDI	Class II	Active
Steri-Drape™	1000	FDA UDI	Class II	Active
Bair Paws™	81501	FDA UDI	Class II	Unknown
3M™ Micropore™	1533-2	FDA UDI	Class I	Active
3M™ Attest™	13915	FDA UDI	Class I	Active
3M™ Nexcare™ Steri-Strip™	H1546	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6202	FDA UDI	Class I	Active
3M™ Littmann® Classic II™	2136	FDA UDI	Class I	Active
Bair Hugger™	81002	FDA UDI	Class II	Active
Filtek™	6028WD	FDA UDI	Class II	Active
3M™ Durapore™	1538-0	FDA UDI	Class I	Active
3m™	EXD-987	FDA UDI	Class I	Unknown
3M™ Filtek™	3740T	FDA UDI	Class I	Active
3M™ Littmann®	2122	FDA UDI	Class I	Active
3M™ ESPE™ Protemp™	50611	FDA UDI	Class I	Active
Red Dot™	2230	FDA UDI	Class II	Active
Futuro™	71065EN	FDA UDI	Class II	Active
3M™ Filtek™	EXD-947167	FDA UDI	Class II	Active
Littmann®	3100NB	FDA UDI	Class II	Active
3M™ Nexcare™	SLT-1	FDA UDI	Class I	Active
3m™	6550XW	FDA UDI	Class II	Active
3M™ Unitek™	900532	FDA UDI	Class I	Active
3M™ Precise™	3995	FDA UDI	Class I	Active
3M™ Filtek™	3700T	FDA UDI	Class I	Active
3m™	1818FS	FDA UDI	Class II	Active
3m™ Espe™	53	FDA UDI	Class I	Active
Filtek™	6020A1	FDA UDI	Class II	Active
Steri-Vac™	GS5-2D	FDA UDI	Class II	Active
3M™ Transpore™	1534-2	FDA UDI	Class I	Active
3M™ ESPE™ Protemp™	50613	FDA UDI	Class I	Active
Attest™	490H	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-44	FDA UDI	Class I	Active
3M™ Tegaderm™	1626W	FDA UDI	Class I	Active
Filtek™	6032OA3	FDA UDI	Class II	Active
3m™ Espe™	EUL3	FDA UDI	Class I	Active
3m™ Espe™	940645	FDA UDI	Class I	Active
3M™ Unitek™	907042	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.