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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 55 of 70

Device	Model / Reference	Registries	Class	Status
3m™	12157C	FDA UDI	Class II	Active
3M™ Red Dot™	2560	FDA UDI	Class II	Active
Steri-Drape™	1079P	FDA UDI	Class II	Active
3M™ ESPE™ Protemp™	50618	FDA UDI	Class I	Active
3m™ Espe™	942301	FDA UDI	Class I	Active
3M™ Red Dot™	2268-5	FDA UDI	Class II	Active
Steri-Vac™	GS8-2D	FDA UDI	Class II	Active
Lava™	2914CN	FDA UDI	Class II	Active
Paradigm™	5511	FDA UDI	Class II	Active
3M™ Unitek™	907026	FDA UDI	Class I	Active
Ioban™ 2	6650EZSB	FDA UDI	Class II	Active
Attest™	41382	FDA UDI	Class II	Active
Steri-Drape™	1192	FDA UDI	Class II	Active
3M™ Cavilon™	3345P	FDA UDI	Class I	Active
Ranger™	24450	FDA UDI	Class II	Unknown
3M™ Tegaderm™	90801	FDA UDI	Class I	Active
Steri-Drape™	1017	FDA UDI	Class II	Active
3M™ Littmann®	6241	FDA UDI	Class I	Active
3m™	1179	FDA UDI	Class II	Active
Steri-Drape™	9010	FDA UDI	Class II	Active
3M™ Micropore™	1533-1	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6201	FDA UDI	Class I	Active
3m™	1500NG	FDA UDI	Class I	Active
Bair Hugger™	63000	FDA UDI	Class II	Active
3M™ RelyX™	3540	FDA UDI	Class I	Active
Filtek™	6028A2B	FDA UDI	Class II	Active
3M™ Aura™	1870+BULK	FDA UDI	Class II	Active
3M™ Unitek™	900441	FDA UDI	Class I	Active
3M™ Nexcare™	W3589	FDA UDI	Class I	Active
Filtek™	6029C3B	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6163	FDA UDI	Class I	Active
3M™ Unitek™	900514	FDA UDI	Class I	Active
Lava™	2614A2-LT	FDA UDI	Class II	Active
Lava™	2012BL-LT	FDA UDI	Class II	Active
3M™ Unitek™	900223	FDA UDI	Class I	Active
3M™ Tegaderm™	90611	FDA UDI	Class I	Active
3M™ Durapore™	1538-2	FDA UDI	Class I	Active
Nova Plus®	7179V	FDA UDI	Class II	Unknown
RelyX™	3505P	FDA UDI	Class II	Active
Bair Hugger™	81201	FDA UDI	Class II	Active
Ioban™ 2	6650	FDA UDI	Class II	Active
3M™ Cavilon™	3344	FDA UDI	Class I	Active
Filtek™	6033A3.5	FDA UDI	Class II	Active
Comply™	1224-0	FDA UDI	Class II	Unknown
Red Dot™	2570-5	FDA UDI	Class II	Active
Comply™ Thermalog™	2134MM	FDA UDI	Class II	Active
3m™ Espe™	940434	FDA UDI	Class I	Active
3m™	1919B	FDA UDI	Class I	Active
3M™ Littmann® Master Cardiology™	2164	FDA UDI	Class I	Active
Steri-Drape™ Ioban™ 2	6659	FDA UDI	Class II	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.