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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
—
Phone
+1(800)634-2249
PRRC Contact
Harry Janiski
EUDAMED SRN
US-MF-000014086
FDA FEI Number
2110898
DUNS Number
830016148

Catalogue (3490)

Page 49 of 70
DeviceModel / ReferenceRegistriesClassStatus
3M™ Littmann® Cardiology IV™ 6165
FDA UDI
Class IActive
3m™ Espe™ DLR4
FDA UDI
Class IActive
3M™ Bair Hugger™ 56000
FDA UDI
Class IIActive
3M™ Steri-Strip™ B1559
FDA UDI
Class IActive
Bair Hugger™ 37000
FDA UDI
Class IIActive
3M™ Littmann® Classic III™ 5862
FDA UDI
Class IActive
3M™ Steri-Strip™ B1551
FDA UDI
Class IActive
3M™ Scotchcast™ WDP4
FDA UDI
Class IActive
Bair Hugger™ 22110
FDA UDI
Class IIActive
3M™ ESPE™ Iso-Form™ U-70
FDA UDI
Class IActive
3M™ Transpore™ 1527-1
FDA UDI
Class IActive
3M™ ESPE™ Iso-Form™ U-54
FDA UDI
Class IActive
E-A-Rlink™ 420-2036
FDA UDI
Class IActive
3M™ Medipore™ 2860S-4
FDA UDI
Class IActive
Futuro™ 71029EN
FDA UDI
Class IIActive
3M™ Transpore™ 1527-3
FDA UDI
Class IActive
3M™ Durapore™ 1590-0
FDA UDI
Class IActive
3M™ Tegaderm™ 1620
FDA UDI
Class IActive
3M™ Red Dot™ 2660-5
FDA UDI
Class IIActive
3M™ Littmann® Classic III™ 5647
FDA UDI
Class IActive
3M™ Steri-Strip™ A1848
FDA UDI
Class IActive
Nova Plus® V2228-3
FDA UDI
Class IIActive
3M™ Littmann® 8890
FDA UDI
Class IIActive
Steri-Drape™ 9085P
FDA UDI
Class IIActive
Lava™ 5074A3-HT
FDA UDI
Class IIActive
3m™ Espe™ 302
FDA UDI
Class IActive
3M™ ESPE™ MDI Classic Intermediate O-Ball 2.1 mm x 18 mm
FDA UDI
Class IIUnknown
3M™ Unitek™ 900535
FDA UDI
Class IActive
3M™ Unitek™ 900237
FDA UDI
Class IActive
3m™ Espe™ 914001
FDA UDI
Class IActive
3M™ Littmann® 2456
FDA UDI
Class IActive
Steri-Drape™ 1082
FDA UDI
Class IIActive
3M™ Unitek™ 900225
FDA UDI
Class IActive
Z100™ 5904A3
FDA UDI
Class IIActive
3m™ 9165L
FDA UDI
Class IIActive
3M™ ESPE™ Iso-Form™ U-71
FDA UDI
Class IActive
3m™ Espe™ ELR4
FDA UDI
Class IActive
3M™ ESPE™ MDI Standard Square Head and Collar 1.8 mm x 15 mm
FDA UDI
Class IIUnknown
3M™ Coban™ 2082S
FDA UDI
Class IActive
RelyX™ 7614WOT
FDA UDI
Class IIActive
Filtek™ 6032B1
FDA UDI
Class IIUnknown
Vanish™ 12150M
FDA UDI
Class IIActive
3M™ Medipore™ 3564
FDA UDI
Class IActive
Filtek™ 6028A2D
FDA UDI
Class IIActive
Comply™ 1322-18MM
FDA UDI
Class IIActive
3M™ Littmann® 6203
FDA UDI
Class IActive
Comply™ 1250
FDA UDI
Class IIActive
Attest™ 115
FDA UDI
Class IIActive
3M™ Cavilon™ 3344
FDA UDI
Class IActive
Imprint™ II Garant™ 9571J
FDA UDI
Class IIActive

Related Companies

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Importers

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Notified Bodies

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Authorities

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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.

DateRecall No.ClassStatusReason
Apr 22, 2025Z-2231-2025—open, classified

Notice was issued to clarify flow rates related to the inlet fluid temperature.

Apr 10, 2025Z-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.