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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 59 of 70

Device	Model / Reference	Registries	Class	Status
Steri-Drape™	1074	FDA UDI	Class II	Active
E-A-Rtone™	410-3018	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6242	FDA UDI	Class I	Active
3M™ Red Dot™	2268-5	FDA UDI	Class II	Active
3M™ Littmann®	8870	FDA UDI	Class II	Active
Ketac™	3305A3.5	FDA UDI	Class II	Active
Paradigm™	3710A3.5	FDA UDI	Class II	Unknown
3M™ Medipore™	2861	FDA UDI	Class I	Active
3M™ Tegaderm™	90704	FDA UDI	Class I	Active
Infant E-A-Rtip	420-2094	FDA UDI	Class I	Active
3M™ Steri-Strip™	R1540	FDA UDI	Class I	Active
Steri-Drape™	1076	FDA UDI	Class II	Active
Steri-Drape™	1062	FDA UDI	Class II	Active
3M™ Medipore™	2860S-4	FDA UDI	Class I	Active
Steri-Drape™	9077R	FDA UDI	Class II	Unknown
3M™ Unitek™	900336	FDA UDI	Class I	Active
3M™ Littmann®	6156	FDA UDI	Class I	Active
Ranger™	24370	FDA UDI	Class II	Active
3M™ Littmann®	2292	FDA UDI	Class I	Active
3M™ Durapore™	1590-1	FDA UDI	Class I	Active
Steri-Drape™	9018	FDA UDI	Class II	Active
Paradigm™	1480OA2	FDA UDI	Class II	Active
Steri-Drape™	1089	FDA UDI	Class II	Active
Bair Hugger™	84202	FDA UDI	Class II	Active
3M™ Tegaderm™	90815	FDA UDI	Class I	Active
3M™ Unitek™	900241	FDA UDI	Class I	Active
Express™	7302	FDA UDI	Class II	Active
3m™ Espe™	LASH	FDA UDI	Class I	Unknown
3M™ Unitek™	900141	FDA UDI	Class I	Active
3m™ Espe™	6UR5	FDA UDI	Class I	Active
Bair Paws™	83002	FDA UDI	Class II	Active
Filtek™	6029B1E	FDA UDI	Class II	Active
Red Dot™	2268-3	FDA UDI	Class II	Active
3M™ Medipore™	3562	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6205	FDA UDI	Class I	Active
3M™ Nexcare™ Transpore™	527-P1	FDA UDI	Class I	Active
Steri-Drape™	9026	FDA UDI	Class II	Active
3M™ Micropore™	1530-1	FDA UDI	Class I	Active
Lava™	3112A3-HT	FDA UDI	Class II	Unknown
3M™ ESPE™ Protemp™	50612	FDA UDI	Class I	Active
Steri-Drape™ Ioban™ 2	6657	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5876	FDA UDI	Class I	Active
3m™ Espe™	940635	FDA UDI	Class I	Active
Steri-Drape™	2065	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-50	FDA UDI	Class I	Active
3M™ Tegaderm™	90817	FDA UDI	Class I	Active
3M Company dba 3M Health Care	2330	FDA UDI	Class II	Active
3m™ Espe™	61	FDA UDI	Class I	Active
3M™ Tegaderm™	1622W	FDA UDI	Class I	Active
3M™ Littmann®	6177	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.