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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 3 of 70

Device	Model / Reference	Registries	Class	Status
3M™ ESPE™ Iso-Form™	U-57	FDA UDI	Class I	Active
3M™ Cavilon™	3346E	FDA UDI	Class I	Active
3m™ Espe™	69	FDA UDI	Class I	Active
Steri-Drape™	9012A	FDA UDI	Class II	Active
Bair Paws™	83103	FDA UDI	Class II	Unknown
Steri-Drape™	1092	FDA UDI	Class II	Active
3m™ Espe™	914022	FDA UDI	Class I	Active
3m™ Espe™	940442	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	U-58	FDA UDI	Class I	Active
Comply™	1322-24MM	FDA UDI	Class II	Active
3M™ Filtek™	6032A3.5	FDA UDI	Class II	Active
3M™ Tegaderm™	90604	FDA UDI	Class I	Active
3M™ Littmann®	2296	FDA UDI	Class I	Active
Express™	7300	FDA UDI	Class II	Active
Steri-Drape™ Ioban™ 2	6697	FDA UDI	Class II	Active
3M™ Steri-Drape™	1035	FDA UDI	Class II	Active
3M™ Bair Hugger™	37000	FDA UDI	Class II	Active
Attest™	1296F	FDA UDI	Class II	Active
Bair Paws™	84102	FDA UDI	Class II	Unknown
3M™ Unitek™	900123	FDA UDI	Class I	Active
Lava™	4714A3-LT	FDA UDI	Class II	Unknown
Fast Release Varnish	12157M	FDA UDI	Class II	Active
3M™ Micropore™	2770-2	FDA UDI	Class I	Active
Steri-Drape™	1084P	FDA UDI	Class II	Active
Paradigm™	2714A3.5-S	FDA UDI	Class II	Active
Attest™	1276	FDA UDI	Class II	Active
3M™ Clinpro™	7200FF	FDA UDI	Class II	Active
3m™	1818	FDA UDI	Class II	Active
Filtek™	6021UD	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5832	FDA UDI	Class I	Active
3M™ Steri-Strip™	R1541	FDA UDI	Class I	Active
3M™ Cavilon™	3343	FDA UDI	Class I	Active
3M™ Unitek™	900224	FDA UDI	Class I	Active
3M™ Tegaderm™	1679	FDA UDI	Class I	Active
Imprint™ II Garant™	9371	FDA UDI	Class II	Active
3M™ Bair Hugger™	30000	FDA UDI	Class II	Active
Filtek™	6028GT	FDA UDI	Class II	Active
Filtek™	6029D2E	FDA UDI	Class II	Active
Bair Paws™	83102	FDA UDI	Class II	Unknown
3M™ Medipore™	2957	FDA UDI	Class I	Active
3M™ Medipore™	3570	FDA UDI	Class I	Active
Steri-Drape™	9045	FDA UDI	Class II	Active
Steri-Drape™	1073	FDA UDI	Class II	Active
Lava™	2614A3.5-LT	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5874	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5812	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5870	FDA UDI	Class I	Active
Nova Plus®	V2244	FDA UDI	Class II	Active
3M™ Micropore™	1535-1	FDA UDI	Class I	Active
Filtek™	4862U	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.