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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 21 of 70
DeviceModel / ReferenceRegistriesClassStatus
3M™ Ioban™ 6651EZ
FDA UDI
Class IIActive
3m™ SPS-YA1010
FDA UDI
Class IActive
3M™ Littmann® 2453
FDA UDI
Class IActive
3M™ Tegaderm™ 16004
FDA UDI
Class IActive
3M™ ESPE™ Iso-Form™ L-67
FDA UDI
Class IActive
3M™ ESPE™ Iso-Form™ U-46
FDA UDI
Class IActive
3M™ Littmann® Cardiology IV™ 6241
FDA UDI
Class IActive
3M™ Medipore™ 2868
FDA UDI
Class IActive
Filtek™ 6029SU
FDA UDI
Class IIActive
Bair Hugger™ 55000
FDA UDI
Class IIActive
3M™ Cavilon™ 3346P
FDA UDI
Class IActive
3M™ Littmann® 8890
FDA UDI
Class IIActive
Steri-Drape™ 9005
FDA UDI
Class IIActive
Express™ 7301
FDA UDI
Class IIActive
3M™ Littmann® Classic III™ 5867
FDA UDI
Class IActive
3M™ Cavilon™ 3345
FDA UDI
Class IActive
Steri-Drape™ 9027L
FDA UDI
Class IIActive
3M™ Littmann® Cardiology IV™ 6178
FDA UDI
Class IActive
3M™ Micropore™ 2770S-2
FDA UDI
Class IActive
3m™ 9661L
FDA UDI
Class IActive
3M™ ESPE™ Iso-Form™ U-74
FDA UDI
Class IActive
3M™ Tegaderm™ 3590
FDA UDI
Class IActive
Filtek™ 6033A1
FDA UDI
Class IIUnknown
Fast Release Varnish 12158M
FDA UDI
Class IIActive
3M™ Tegaderm™ 1634
FDA UDI
Class IActive
Paradigm™ 1481A4
FDA UDI
Class IIActive
Vitremer™ 3303MP BLUE
FDA UDI
Class IIActive
Express™ 7302T
FDA UDI
Class IIActive
3M™ ESPE™ MDI Standard O-Ball and Collar 1.8 mm x 10 mm
FDA UDI
Class IIActive
Z100™ 5905C2
FDA UDI
Class IIActive
3M™ Tegaderm™ 90802
FDA UDI
Class IActive
3M™ Bair Hugger™ 54200
FDA UDI
Class IIActive
3M™ Littmann® Master Cardiology™ 2161
FDA UDI
Class IActive
3M™ Littmann® Master Cardiology™ 2163
FDA UDI
Class IActive
3M™ Littmann® Classic III™ 5868
FDA UDI
Class IActive
3M™ Steri-Strip™ C1544
FDA UDI
Class IActive
3M™ Bair Hugger™ 77500
FDA UDI
Class IIActive
Red Dot™ 2660-3
FDA UDI
Class IIActive
Filtek™ 6029CT
FDA UDI
Class IIActive
3M™ Blenderm™ 1525-1
FDA UDI
Class IActive
Lava™ 3112A1-LT
FDA UDI
Class IIUnknown
3M™ Medipore™ 2964S
FDA UDI
Class IActive
3M™ Nexcare™ 571-08
FDA UDI
Class IActive
Bair Hugger™ 31500
FDA UDI
Class IIActive
Lava™ 2914B1-HT
FDA UDI
Class IIActive
Ranger™ 24500
FDA UDI
Class IIActive
3m™ 9130
FDA UDI
Class IIActive
Red Dot™ 2249-50
FDA UDI
Class IIActive
3M™ Filtek™ 6550A3
FDA UDI
Class IIActive
3M™ Steri-Drape™ 2040
FDA UDI
Class IIActive

Related Companies

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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.