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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 57 of 70

Device	Model / Reference	Registries	Class	Status
3m™ Espe™	DUR2	FDA UDI	Class I	Active
Steri-Drape™	1027	FDA UDI	Class II	Active
3M™ Nexcare™ Tegaderm™	TEGA-10	FDA UDI	Class I	Active
3M™ Medipore™	3569	FDA UDI	Class I	Active
3M™ Tegaderm™	1623W	FDA UDI	Class I	Active
3M™ Nexcare™	731-SIOC	FDA UDI	Class I	Active
3m™ Espe™	940325	FDA UDI	Class I	Active
3m™ Espe™	DLR6	FDA UDI	Class I	Active
Z100™	5907P	FDA UDI	Class II	Active
3M™ Medipore™	2860-6	FDA UDI	Class I	Active
3M™ Tegaderm™	9543HP	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6232	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6234	FDA UDI	Class I	Active
Comply™	1248	FDA UDI	Class II	Active
3M™Filtek™	6110S	FDA UDI	Class II	Active
3M™ Filtek™	EXD-947167	FDA UDI	Class II	Active
3M™ Steri-Vac™	GS8-2D	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6176	FDA UDI	Class I	Active
Attest™	1264	FDA UDI	Class II	Active
Express™	7314	FDA UDI	Class II	Active
Adper™ Scotchbond™	7547	FDA UDI	Class II	Unknown
3m™ Espe™	60	FDA UDI	Class I	Active
3M™ Micropore™	1530-254	FDA UDI	Class I	Active
Lava™	3112A3.5-LT	FDA UDI	Class II	Unknown
3M™ Littmann® Master Cardiology™	2182	FDA UDI	Class I	Active
Paradigm™	1480B2	FDA UDI	Class II	Active
3M™ ESPE™ Protemp™	50600TK	FDA UDI	Class I	Active
3M™ Filtek™	6550A4	FDA UDI	Class II	Active
3M™ Micropore™	1530-136	FDA UDI	Class I	Active
3m™ Espe™	1919F	FDA UDI	Class I	Active
3M™ Littmann®	8863	FDA UDI	Class II	Active
3M™ Unitek™	900446	FDA UDI	Class I	Active
Paradigm™	1481A3.5	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6156	FDA UDI	Class I	Active
E-A-Rlink™	420-2005	FDA UDI	Class I	Active
3m™ Espe™	940542	FDA UDI	Class I	Active
3m™ Espe™	6UR6	FDA UDI	Class I	Active
3M™ Unitek™	900327	FDA UDI	Class I	Active
Paradigm™	1480B3	FDA UDI	Class II	Active
Steri-Drape™	9085W	FDA UDI	Class II	Active
3M™ Transpore™	1527-2	FDA UDI	Class I	Active
Bair Hugger™	31000	FDA UDI	Class II	Active
E-A-Rlink™	420-2004	FDA UDI	Class I	Active
Steri-Drape™	9000L	FDA UDI	Class II	Active
3M™ Red Dot™	2560-5	FDA UDI	Class II	Active
Bair Hugger™	36000	FDA UDI	Class II	Active
3m™ Espe™	940445	FDA UDI	Class I	Active
Lava™	2914B1-LT	FDA UDI	Class II	Active
E-A-Rlink™	420-2087	FDA UDI	Class I	Active
RelyX™	8716	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.