Is this your brand? Sign in to claim ownership.

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 12 of 70

Device	Model / Reference	Registries	Class	Status
Red Dot™	2360	FDA UDI	Class II	Active
3M™ Filtek™	6550A2-S	FDA UDI	Class II	Active
3M™ Bair Hugger™	30500	FDA UDI	Class II	Active
3M™ Tegaderm™	9536HP	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5807	FDA UDI	Class I	Active
3M™ ESPE™ MDI Max with O-Ball Head and Collar	2.4 mm x 15 mm	FDA UDI	Class II	Unknown
3M™ Unitek™	900545	FDA UDI	Class I	Active
3m™ Espe™	6LL4	FDA UDI	Class I	Active
3M™ Littmann®	5839	FDA UDI	Class I	Active
3m™ Espe™	18	FDA UDI	Class I	Active
3m™ Espe™	940346	FDA UDI	Class I	Active
Lava™	1314A2-LT	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6232	FDA UDI	Class I	Active
Steri-Drape™	1081	FDA UDI	Class II	Active
3M™ Medipore™	3566	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6158	FDA UDI	Class I	Active
3M™ Littmann®	8483	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5626	FDA UDI	Class I	Active
3m™ Espe™	940512	FDA UDI	Class I	Active
3M™ Tegaderm™	9505W	FDA UDI	Class I	Active
3M™ Unitek™	900434	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5627	FDA UDI	Class I	Active
Steri-Drape™	9051	FDA UDI	Class II	Active
3M™ Littmann®	6180	FDA UDI	Class I	Active
3M™ Coban™	2083S	FDA UDI	Class I	Active
3m™ Espe™	DLL5	FDA UDI	Class I	Active
3M™ Nexcare™	FPT-05	FDA UDI	Class I	Active
3M™ Filtek™	6032A2	FDA UDI	Class II	Active
Red Dot™	2271-5	FDA UDI	Class II	Active
3M™ Steri-Strip™	R1546	FDA UDI	Class I	Active
3M™ Tegaderm™	90612	FDA UDI	Class I	Active
Filtek™	6029GT	FDA UDI	Class II	Active
Filtek™	6033A3	FDA UDI	Class II	Active
Filtek™	6028C2B	FDA UDI	Class II	Active
3M™ Bair Hugger™	53000	FDA UDI	Class II	Active
3m™ Espe™	940322	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	L-62	FDA UDI	Class I	Active
Filtek™	6029A2B	FDA UDI	Class II	Active
Ranger™	24533	FDA UDI	Class II	Unknown
Bair Hugger™	90133	FDA UDI	Class II	Unknown
Bair Hugger™	90055	FDA UDI	Class II	Active
3M™ Micropore™	1532S-1	FDA UDI	Class I	Active
3m™	9667L-E	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5624	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5629	FDA UDI	Class I	Active
3M™ Filtek™	6555A2	FDA UDI	Class II	Active
Steri-Drape™	9196	FDA UDI	Class II	Active
3M™ Transpore™	1527-118	FDA UDI	Class I	Active
3m™ Espe™	101	FDA UDI	Class I	Active
Bair Hugger™	64500	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.