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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 19 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Steri-Strip™	W8512	FDA UDI	Class I	Active
3M™ Bair Hugger™	55501	FDA UDI	Class II	Active
3M™ ESPE™ MDI Max with an O-Ball Head	2.4 mm x 10 mm	FDA UDI	Class II	Unknown
Steri-Drape™	9007	FDA UDI	Class II	Active
3M™ Red Dot™	2231	FDA UDI	Class II	Active
3m™	9681	FDA UDI	Class I	Active
3M™ Littmann®	6240	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5633	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5869	FDA UDI	Class I	Active
Espe™	1322F	FDA UDI	Class II	Unknown
3M™ Medipore™	2860S-6	FDA UDI	Class I	Active
3M™ Attest™	41382	FDA UDI	Class II	Active
3m™	9667L-A	FDA UDI	Class I	Active
3M™ Littmann®	8493	FDA UDI	Class II	Active
Attest™	1276F	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-65	FDA UDI	Class I	Active
Filtek™	6029B1B	FDA UDI	Class II	Active
Lava™	5072A3-HT	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-63	FDA UDI	Class I	Active
3m™	MS01	FDA UDI	Class I	Active
Attest™	1261P	FDA UDI	Class II	Unknown
3m™ Espe™	940323	FDA UDI	Class I	Active
3M™ Micropore™	2770-2	FDA UDI	Class I	Active
3M™ Littmann®	2119	FDA UDI	Class I	Active
Lava™	1314A3.5-LT	FDA UDI	Class II	Active
3M™ Littmann®	6176	FDA UDI	Class I	Active
Lava™	5044D2-LT	FDA UDI	Class II	Unknown
Steri-Drape™ Ioban™ 2	6682	FDA UDI	Class II	Active
3m™ Espe™	940540	FDA UDI	Class I	Active
3M™ Tegaderm™	1626W	FDA UDI	Class I	Active
Red Dot™	2289PAL	FDA UDI	Class II	Active
3M™ Red Dot™	2330	FDA UDI	Class II	Active
Paradigm™	2710E-S	FDA UDI	Class II	Unknown
3M™ Littmann®	5868	FDA UDI	Class I	Active
3M™ Ioban™	6640EZ	FDA UDI	Class II	Active
3M™ Durapore™	1538-2D	FDA UDI	Class I	Active
Filtek™	6029BT	FDA UDI	Class II	Active
3M™ Unitek™	900541	FDA UDI	Class I	Active
3M™ Steri-Drape™ Cardiovascular Sheet with Ioban™	6681	FDA UDI	Class II	Active
3M™ Ranger™	24370	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5832	FDA UDI	Class I	Active
Attest™	1294	FDA UDI	Class II	Active
3M™ Steri-Strip™	A1847	FDA UDI	Class I	Active
3m™	1818	FDA UDI	Class II	Active
3M™ Unitek™	900645	FDA UDI	Class I	Active
Ioban™ 2	6648EZ	FDA UDI	Class II	Active
3M™ Unitek™ Temporary Anchorage Device (TAD) TAD Introductory Kit	504-101	FDA UDI	Class II	Active
3m™ Espe™	940345	FDA UDI	Class I	Active
3M™ ESPE™ MDI Max with an O-Ball Head	2.4 mm x 13 mm	FDA UDI	Class II	Unknown
Lava™	5044B1-HT	FDA UDI	Class II	Unknown

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.