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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 9 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Unitek™	900524	FDA UDI	Class I	Active
3M™ Unitek™	900137	FDA UDI	Class I	Active
SpotOn™	36000	FDA UDI	Class II	Active
Lava™	3114B1-LT	FDA UDI	Class II	Active
3M™ Unitek™	900116	FDA UDI	Class I	Active
3M™ Littmann™	8493	FDA UDI	Class II	Active
Paradigm™	1481B3	FDA UDI	Class II	Active
Lava™	2914A1-HT	FDA UDI	Class II	Active
3m™ Espe™	DUR3	FDA UDI	Class I	Active
Bair Hugger™	30500	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-69	FDA UDI	Class I	Active
Lava™	1334A1-LT	FDA UDI	Class II	Unknown
3M™ ESPE™ Protemp™	50615	FDA UDI	Class I	Active
3m™ Espe™	940436	FDA UDI	Class I	Active
3M™ Littmann®	2451	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6200	FDA UDI	Class I	Active
E-A-Rlink™	420-2006	FDA UDI	Class I	Active
3M™ Tegaderm™	3586	FDA UDI	Class I	Active
Steri-Drape™	2051	FDA UDI	Class II	Active
"3M™ ESPE™ MDI Max with Square Head and Collar	2.4 mm x 15 mm	FDA UDI	Class II	Unknown
Ranger™	24240	FDA UDI	Class II	Active
3M™ Transpore™	1534S-1	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	U-75	FDA UDI	Class I	Active
3M™ Nexcare™ Durapore™	538-P2	FDA UDI	Class I	Active
Lava™	3112B1-HT	FDA UDI	Class II	Unknown
3M™ Bair Hugger™	61000	FDA UDI	Class II	Active
3M™ Steri-Strip™	R1549	FDA UDI	Class I	Active
3m™ Espe™	6UL3	FDA UDI	Class I	Active
Paradigm™	5313J	FDA UDI	Class II	Active
3M™ Unitek™	907012	FDA UDI	Class I	Active
3M™ Micropore™	1530-2	FDA UDI	Class I	Active
3M™ Filtek™	6555-SK	FDA UDI	Class II	Active
3M™ Attest™	1243A	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6234	FDA UDI	Class I	Active
Bair Hugger™	84101	FDA UDI	Class II	Active
Attest™	1262	FDA UDI	Class II	Active
Ioban™ 2	6651EZSB	FDA UDI	Class II	Active
Filtek™	4862A1	FDA UDI	Class II	Active
Bair Hugger™	54000	FDA UDI	Class II	Active
3M™ ESPE™ MDI O-Ball Prosthetic Head	1.8 mm x 18 mm	FDA UDI	Class II	Unknown
Lava™	5072D2-LT	FDA UDI	Class II	Active
Littmann®	3200NB	FDA UDI	Class II	Active
3M™ Littmann®	2301	FDA UDI	Class I	Active
3M™ ACE™ Brand	906001	FDA UDI	Class I	Active
3m™ Espe™	6UL7	FDA UDI	Class I	Active
Z100™	5905B2	FDA UDI	Class II	Active
Futuro™	71037EN	FDA UDI	Class II	Active
Lava™	5074A3-LT	FDA UDI	Class II	Active
3m™ Espe™	ELR6	FDA UDI	Class I	Active
Paradigm™	2714A3-S	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.