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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 6 of 70
DeviceModel / ReferenceRegistriesClassStatus
Bair Hugger™ 83103
FDA UDI
Class IIActive
3M™ Medipore™ 2860S-2
FDA UDI
Class IActive
3M™ Bair Hugger™ 81003
FDA UDI
Class IIActive
Filtek™ 6029CP
FDA UDI
Class IIActive
3m™ Espe™ 2920
FDA UDI
Class IUnknown
Paradigm™ 1481B2
FDA UDI
Class IIActive
3M™ ESPE™ Iso-Form™ U-50
FDA UDI
Class IActive
3m™ Espe™ 1919B
FDA UDI
Class IActive
3M™ ESPE™ Iso-Form™ L-58
FDA UDI
Class IActive
3M™ Medipore™ 3562
FDA UDI
Class IActive
3M™ Tegaderm™ 1626
FDA UDI
Class IActive
3M™ Durapore™ 1590B-136
FDA UDI
Class IActive
3m™ Espe™ DLL6
FDA UDI
Class IActive
3M™ Tegaderm™ 1616
FDA UDI
Class IActive
3M™ Precise™ DS-5
FDA UDI
Class IActive
3M™ Nexcare™ CCT-05
FDA UDI
Class IActive
3M™ Littmann® Classic III™ 5811
FDA UDI
Class IActive
3M™ Tegaderm™ 90601
FDA UDI
Class IActive
3M™ Tegaderm™ 90642
FDA UDI
Class IActive
Steri-Drape™ 9000
FDA UDI
Class IIActive
3M™ ESPE™ Iso-Form™ BC64
FDA UDI
Class IActive
Filtek™ 4861U
FDA UDI
Class IIActive
Bair Paws™ 84202
FDA UDI
Class IIUnknown
Filtek™ 6032D2
FDA UDI
Class IIUnknown
3M™ Littmann® Classic III™ 5960
FDA UDI
Class IActive
3M™ Nexcare™ 779
FDA UDI
Class IActive
Ranger™ 29700
FDA UDI
Class IActive
3M™ Unitek™ 900214
FDA UDI
Class IActive
Filtek™ 6021B2
FDA UDI
Class IIActive
Filtek™ 6028C1B
FDA UDI
Class IIActive
Filtek™ 6029C4D
FDA UDI
Class IIActive
3m™ Espe™ 940520
FDA UDI
Class IActive
Steri-Drape™ 9090
FDA UDI
Class IIActive
3M™ Unitek™ 900212
FDA UDI
Class IActive
Bair Paws™ 81101
FDA UDI
Class IIActive
3M™ Comply™ 13915
FDA UDI
Class IActive
3M™ Littmann® Classic III™ 5863
FDA UDI
Class IActive
Bair Hugger™ Novaplus™ 40034
FDA UDI
Class IIActive
Bair Paws™ 81103
FDA UDI
Class IIUnknown
Filtek™ 6028B1B
FDA UDI
Class IIActive
3m™ 78001
FDA UDI
Class IIUnknown
3M™ Filtek™ 6550B1
FDA UDI
Class IIActive
Filtek™ 6029B3D
FDA UDI
Class IIActive
3m™ 1860S
FDA UDI
Class IIActive
Ranger™ 24355
FDA UDI
Class IIActive
Curos™ CFF10-250N
FDA UDI
UActive
Lava™ 3112B1-LT
FDA UDI
Class IIUnknown
3m™ Espe™ ELL5
FDA UDI
Class IActive
Filtek™ 6029PP
FDA UDI
Class IActive
Tegaderm™ 90307
FDA UDI
UActive

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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.