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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 60 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Tegaderm™	1624W	FDA UDI	Class I	Active
Paradigm™	2714A2-S	FDA UDI	Class II	Active
Bair Hugger™	56000	FDA UDI	Class II	Unknown
3M™ Littmann®	2164	FDA UDI	Class I	Active
3M™ Steri-Strip™	W8516	FDA UDI	Class I	Active
Steri-Drape™	9050P	FDA UDI	Class II	Active
Lava™	2614A1-HT	FDA UDI	Class II	Active
3M™ ESPE™ MDI Max with Square Head and Collar	2.4 mm x 10 mm	FDA UDI	Class II	Unknown
Bair Hugger™	90131	FDA UDI	Class II	Active
3M™ Unitek™	900333	FDA UDI	Class I	Active
3M™ Red Dot™	2360	FDA UDI	Class II	Active
Filtek™	4867A2	FDA UDI	Class II	Active
Lava™	5044A3.5-LT	FDA UDI	Class II	Unknown
Nova Plus®	9165V	FDA UDI	Class II	Unknown
3M™ Steri-Drape™	9095	FDA UDI	Class II	Active
3m™ Espe™	940343	FDA UDI	Class I	Active
3M™ Littmann®	5959	FDA UDI	Class I	Active
Lava™	1334A3.5-LT	FDA UDI	Class II	Unknown
3M™ Unitek™	907001	FDA UDI	Class I	Active
3M™ Ranger™	24450	FDA UDI	Class II	Active
Lava™	2914A2-LT	FDA UDI	Class II	Active
3M™ Unitek™	900312	FDA UDI	Class I	Active
Filtek™	6029D3B	FDA UDI	Class II	Active
3M™ Tegaderm™	9534HP	FDA UDI	Class I	Active
3m™ Espe™	6UR7	FDA UDI	Class I	Active
RelyX™	8716TK	FDA UDI	Class II	Active
3M™ Nexcare™ Micropore™	530-P1/2	FDA UDI	Class I	Active
3M™ Littmann® Classic II™	2114	FDA UDI	Class I	Active
Filtek™	4867A3	FDA UDI	Class II	Active
3M™ Durapore™	1538-1D	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6179	FDA UDI	Class I	Active
Bair Hugger™	79500	FDA UDI	Class II	Unknown
Bair Hugger™	81203	FDA UDI	Class II	Active
Adper™	51101	FDA UDI	Class II	Active
Paradigm™	2714B3-S	FDA UDI	Class II	Active
Z100™	5905A3.5	FDA UDI	Class II	Active
Filtek™	6028AT	FDA UDI	Class II	Active
3M™ Transpore™	1534-2	FDA UDI	Class I	Active
3M™ Durapore™	1538-1D	FDA UDI	Class I	Active
3M™ Red Dot™	2570-5	FDA UDI	Class II	Active
Steri-Drape™	9050	FDA UDI	Class II	Active
3M™ Littmann®	2113R	FDA UDI	Class I	Active
3M™ Durapore™	1548S-1	FDA UDI	Class I	Active
Paradigm™	5514S	FDA UDI	Class II	Active
Lava™	1314B1-HT	FDA UDI	Class II	Active
3M™ Unitek™	900132	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6166	FDA UDI	Class I	Active
3M™ Cavilon™	3343K	FDA UDI	Class I	Active
3m™ Espe™	800417	FDA UDI	Class I	Active
3m™ Espe™	20	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.