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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 53 of 70

Device	Model / Reference	Registries	Class	Status
3M™ ESPE™ MDI Standard O-Ball and Collar	1.8 mm x 13 mm	FDA UDI	Class II	Unknown
3M™ Littmann®	2157	FDA UDI	Class I	Active
3M™ Steri-Strip™	R1540	FDA UDI	Class I	Active
3m™	9682	FDA UDI	Class I	Active
3M™ Tegaderm™	90640	FDA UDI	Class I	Active
3M™ Tegaderm™	90007	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6159	FDA UDI	Class I	Active
3m™ Espe™	C-180	FDA UDI	Class I	Active
3m™ Espe™	0550-10	FDA UDI	Class I	Unknown
Vitremer™	3303FG	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-49	FDA UDI	Class I	Active
3M™ Unitek™	900217	FDA UDI	Class I	Active
E-A-Rtone™	410-3016	FDA UDI	Class II	Active
3m™ Espe™	6LL2	FDA UDI	Class I	Active
3M™ Unitek™	907005	FDA UDI	Class I	Active
3M™ Tegaderm™	90602	FDA UDI	Class I	Active
Z100™	5905A3	FDA UDI	Class II	Active
3m™	9660	FDA UDI	Class I	Active
Tegaderm™	1660	FDA UDI	U	Active
Bair Hugger™	83102	FDA UDI	Class II	Active
Lava™	3112BL-LT	FDA UDI	Class II	Unknown
3M™ Multipore™	3730-0	FDA UDI	Class I	Active
3M™ Ranger™	24750	FDA UDI	Class II	Active
3M™ Steri-Strip™	E4541	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	U-78	FDA UDI	Class I	Active
Nova Plus®	V2237	FDA UDI	Class II	Active
Nova Plus®	V2237-5	FDA UDI	Class II	Unknown
3M™ Comply™	13913	FDA UDI	Class I	Active
Ranger™	24200	FDA UDI	Class II	Unknown
3M™ Unitek™	907051	FDA UDI	Class I	Active
3M™ Steri-Drape™	1051	FDA UDI	Class II	Active
Steri-Drape™	1051	FDA UDI	Class II	Active
Vitremer™	3303I	FDA UDI	Class II	Active
Steri-Drape™	9012L	FDA UDI	Class II	Active
3M™ Transpore™	1534-1	FDA UDI	Class I	Active
3M™ Littmann® Classic II™	2122	FDA UDI	Class I	Active
Lava™	2914BL-LT	FDA UDI	Class II	Active
3m™ Espe™	DUL7	FDA UDI	Class I	Active
3M™ Multipore™	3730-0	FDA UDI	Class I	Active
3M™ Littmann® Master Cardiology™	2178	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6153	FDA UDI	Class I	Active
Steri-Drape™ Ioban™ 2	6619P001	FDA UDI	Class II	Active
Steri-Drape™	9062	FDA UDI	Class II	Active
Lava™	3114A1-LT	FDA UDI	Class II	Active
3M™ ESPE™ MDI Max with an O-Ball Head	2.4 mm x 15 mm	FDA UDI	Class II	Unknown
3M™ Steri-Drape™	1064	FDA UDI	Class II	Active
Steri-Drape™	9015	FDA UDI	Class II	Active
3M™ Steri-Strip™	E4540	FDA UDI	Class I	Active
Filtek™	6032B2	FDA UDI	Class II	Unknown
3M™ Red Dot™	2670-3	FDA UDI	Class II	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.