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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 51 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Clinpro™	7200W	FDA UDI	Class II	Active
3M™ Steri-Drape™	1055B	FDA UDI	Class II	Active
3M™ Filtek™	EXD-947167	FDA UDI	Class II	Active
Lava™	5072A1-LT	FDA UDI	Class II	Active
3M™ Steri-Drape™	1040	FDA UDI	Class II	Active
Clinpro™	12621MW	FDA UDI	Class II	Active
3m™	EXD949OP	FDA UDI	Class II	Active
3M™ Tegaderm™	1689	FDA UDI	Class I	Active
3m™	78011	FDA UDI	Class II	Active
3m™ Espe™	33	FDA UDI	Class I	Active
3M™ Steri-Strip™	A1846	FDA UDI	Class I	Active
3M™ Littmann®	8839	FDA UDI	Class II	Active
3M™ ACE™ Brand	900138	FDA UDI	Class I	Active
Steri-Drape™	1009	FDA UDI	Class II	Unknown
Steri-Drape™	9031	FDA UDI	Class II	Active
3M™ Tegaderm™	3584	FDA UDI	Class I	Active
3M™ Tegaderm™	90610	FDA UDI	Class I	Active
3M™ Littmann® Master Classic II™	2144L	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6187C	FDA UDI	Class I	Active
Red Dot™	9640	FDA UDI	Class II	Active
Lava™	3112C2-LT	FDA UDI	Class II	Unknown
3m™ Espe™	940311	FDA UDI	Class I	Active
Express™	6160J	FDA UDI	Class II	Active
Bair Hugger™	31500	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-59	FDA UDI	Class I	Active
3M™ Unitek™	900534	FDA UDI	Class I	Active
Tegaderm™	90500	FDA UDI	U	Active
Attest™	41380	FDA UDI	Class II	Active
3m™	6550B2	FDA UDI	Class II	Active
3m™ Espe™	34	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6152	FDA UDI	Class I	Active
3m™ Espe™	940544	FDA UDI	Class I	Active
3m™ Espe™	27	FDA UDI	Class I	Active
Bair Hugger™	58501	FDA UDI	Class II	Active
Bair Hugger™	22110	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2113	FDA UDI	Class I	Active
Filtek™	6028A1E	FDA UDI	Class II	Active
Steri-Drape™	9008A	FDA UDI	Class II	Active
Steri-Drape™ Ioban™ 2	6658	FDA UDI	Class II	Active
3M™ Micropore™	1530S-2	FDA UDI	Class I	Active
Comply™	3983MM	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2179	FDA UDI	Class I	Active
Ranger™	24533	FDA UDI	Class II	Unknown
Paradigm™	5515	FDA UDI	Class II	Active
Futuro™	71046EN	FDA UDI	Class II	Active
Lava™	2912C2-LT	FDA UDI	Class II	Active
Filtek™	6028A4B	FDA UDI	Class II	Active
Ranger™	24250	FDA UDI	Class II	Active
Filtek™	4864A2	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-54	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.