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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 20 of 70

Device	Model / Reference	Registries	Class	Status
Lava™	3114SK	FDA UDI	Class II	Unknown
RelyX™	7614B0.5	FDA UDI	Class II	Active
Imprint™ II Garant™	9378	FDA UDI	Class II	Active
3M™ Tegaderm™	90702	FDA UDI	Class I	Active
Express™	7301T	FDA UDI	Class II	Active
3M™ Medipore™	2958	FDA UDI	Class I	Active
Tegaderm™	79-2100K01	FDA UDI	U	Active
3M™ Tegaderm™	90800	FDA UDI	Class I	Active
E-A-Rtone™	410-3010	FDA UDI	Class II	Active
3M™ Medipore™	3564	FDA UDI	Class I	Active
3M™ Steri-Strip™	E4548	FDA UDI	Class I	Active
3M™ Medipore™	2866S	FDA UDI	Class I	Active
Filtek™	6028A3B	FDA UDI	Class II	Active
Filtek™	4864A2-S	FDA UDI	Class II	Active
Red Dot™	2670-5	FDA UDI	Class II	Active
Lava™	2912A3-HT	FDA UDI	Class II	Active
Lava™	2914SK	FDA UDI	Class II	Active
3M™ Nexcare™	CB203	FDA UDI	Class I	Active
3M™ Cavilon™	3346N	FDA UDI	Class I	Active
3M™ Nexcare™	556-25	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6203	FDA UDI	Class I	Active
3M™ Red Dot™	2660-3	FDA UDI	Class II	Active
3M™ Cavilon™	3344E	FDA UDI	Class I	Active
3M™ Cavilon™	3343P	FDA UDI	Class I	Active
3m™ Espe™	940446	FDA UDI	Class I	Active
Lava™	2914A3-LT	FDA UDI	Class II	Active
Bair Hugger™	30500	FDA UDI	Class II	Active
Steri-Drape™	1080	FDA UDI	Class II	Active
Lava™	2614D2-LT	FDA UDI	Class II	Active
3M™ Micropore™	1533-0	FDA UDI	Class I	Active
Bair Hugger™	90133	FDA UDI	Class II	Active
3M™ Littmann®	2176	FDA UDI	Class I	Active
3M™ Littmann®	6183	FDA UDI	Class I	Active
3M™ Tegaderm™	90604	FDA UDI	Class I	Active
3M™ Nexcare™ Active™	516-30PB	FDA UDI	Class I	Active
Steri-Drape™	2045	FDA UDI	Class II	Active
3M™ Littmann®	2454	FDA UDI	Class I	Active
3M™ Precise™	PGX-15W	FDA UDI	Class I	Active
3M™ Unitek™	900513	FDA UDI	Class I	Active
3M™ Unitek™	900631	FDA UDI	Class I	Active
3M™ Nexcare™	527-20CB	FDA UDI	Class I	Active
3M™ Littmann®	5861	FDA UDI	Class I	Active
Steri-Drape™	1115	FDA UDI	Class II	Active
Bair Hugger™	30000	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6162	FDA UDI	Class I	Active
Steri-Drape™	9077R	FDA UDI	Class II	Active
3m™ Espe™	EUR3	FDA UDI	Class I	Active
3m™ Espe™	6LR2	FDA UDI	Class I	Active
3M™ Unitek™	907045	FDA UDI	Class I	Active
Attest™	1278F	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.