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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 2 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Littmann® Classic III™	5620	FDA UDI	Class I	Active
Ranger™	24200	FDA UDI	Class II	Active
3M™ Nexcare™	581-08	FDA UDI	Class I	Active
3M™ Tegaderm™	5643	FDA UDI	Class I	Active
3m™	9600	FDA UDI	Class I	Active
3M™ Filtek™	749-400	FDA UDI	Class I	Active
Lava™	5044BL-LT	FDA UDI	Class II	Unknown
3m™	21174	FDA UDI	Class II	Active
3m™	1180	FDA UDI	Class II	Active
3M™ Unitek™	907035	FDA UDI	Class I	Active
3m™	6550PO	FDA UDI	Class II	Active
3m™	2228-3	FDA UDI	Class II	Active
3M™ Unitek™	900236	FDA UDI	Class I	Active
Lava™	2914D2-LT	FDA UDI	Class II	Active
Steri-Drape™	1194	FDA UDI	Class II	Active
Filtek™	4862A2	FDA UDI	Class II	Active
Bair Hugger™	77500	FDA UDI	Class II	Active
Comply™	6600	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6171	FDA UDI	Class I	Active
3M™ Littmann®	5875	FDA UDI	Class I	Active
3M™ Microfoam™	1528-3	FDA UDI	Class I	Active
Filtek™	6028C3B	FDA UDI	Class II	Active
3M™ Tegaderm™	3582	FDA UDI	Class I	Active
3M™ Unitek™	900247	FDA UDI	Class I	Active
3m™	1835	FDA UDI	Class II	Active
Bair Paws™	81102	FDA UDI	Class II	Unknown
Steri-Drape™	1061	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5829	FDA UDI	Class I	Active
3m™ Espe™	100	FDA UDI	Class I	Active
Steri-Drape™	1191	FDA UDI	Class II	Active
3m™	9667L	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6241	FDA UDI	Class I	Active
Red Dot™	2238-5	FDA UDI	Class II	Active
Red Dot™	2282L	FDA UDI	Class II	Active
3M™ Nexcare™	588-20PB	FDA UDI	Class I	Active
3M™ Tegaderm™	1679NS	FDA UDI	Class I	Active
3M™ Unitek™	907054	FDA UDI	Class I	Active
3M™ Littmann®	6183	FDA UDI	Class I	Active
3M™ Littmann® Classic II™	2119	FDA UDI	Class I	Active
3M™ Tegaderm™	90613	FDA UDI	Class I	Active
E-A-Rlink™	420-2028	FDA UDI	Class I	Active
3M™ Littmann® Master Classic II™	2147	FDA UDI	Class I	Active
Steri-Drape™ Ioban™ 2	6677P	FDA UDI	Class II	Active
3M™ Steri-Strip™	R1541	FDA UDI	Class I	Active
3m™	1501U	FDA UDI	Class I	Active
3M™ Unitek™	907015	FDA UDI	Class I	Active
3m™	9690	FDA UDI	Class I	Active
Filtek™	6033XW	FDA UDI	Class II	Unknown
3M™ Steri-Drape™ Cardiovascular Pack with Ioban™	6677P	FDA UDI	Class II	Active
3M™ Littmann®	8575	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.