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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 50 of 70

Device	Model / Reference	Registries	Class	Status
3M™ ESPE™ Iso-Form™	L-79	FDA UDI	Class I	Active
Filtek™	6029B2E	FDA UDI	Class II	Active
Red Dot™	2248-50	FDA UDI	Class II	Active
3M™ Durapore™	1590-3	FDA UDI	Class I	Active
Futuro™	71038EN	FDA UDI	Class II	Active
3M™ Cavilon™	3344ENS	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	U-53	FDA UDI	Class I	Active
3m™	21172	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5864	FDA UDI	Class I	Active
Bair Hugger™	54500	FDA UDI	Class II	Active
3M™ Unitek™	900126	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	L-74	FDA UDI	Class I	Active
Lava™	1334B1-LT	FDA UDI	Class II	Unknown
3M™ Steri-Strip™	E4546	FDA UDI	Class I	Active
Lava™	3114D2-LT	FDA UDI	Class II	Active
3M™ Unitek™	900122	FDA UDI	Class I	Active
3M™ Tegaderm™	1633	FDA UDI	Class I	Active
3M™ Microfoam™	1528-1	FDA UDI	Class I	Active
3M™ Littmann®	2114R	FDA UDI	Class I	Active
Filtek™	6028B2B	FDA UDI	Class II	Active
Scothbond™	7423	FDA UDI	Class II	Active
Filtek™	6029A3.5B	FDA UDI	Class II	Active
3M™ Tegaderm™	90800	FDA UDI	Class I	Active
3M™ Unitek™	900222	FDA UDI	Class I	Active
3M™ Littmann®	5832	FDA UDI	Class I	Active
3M™ Unitek™	900525	FDA UDI	Class I	Active
3m™ Espe™	31	FDA UDI	Class I	Active
3M™ Red Dot™	2570-3	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6158	FDA UDI	Class I	Active
3M™ Unitek™	907021	FDA UDI	Class I	Active
3M™ Unitek™	900442	FDA UDI	Class I	Active
3M™ Cavilon™	3342	FDA UDI	Class I	Active
3M™ Filtek™	6032C2	FDA UDI	Class II	Active
3M™ Tegaderm™	1685	FDA UDI	Class I	Active
Attest™	1491	FDA UDI	Class II	Active
Steri-Drape™	1135	FDA UDI	Class II	Active
3M™ Unitek™	900510	FDA UDI	Class I	Active
3M™ Medipore™	2860S-6	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5630	FDA UDI	Class I	Active
3m™ Espe™	77581	FDA UDI	Class II	Active
3m™ Espe™	6LL3	FDA UDI	Class I	Active
3M™ Tegaderm™	1629	FDA UDI	Class I	Active
Littmann®	3200NB	FDA UDI	Class II	Active
3m™ Espe™	41	FDA UDI	Class I	Active
3M™ Tegaderm™	90615	FDA UDI	Class I	Active
3M™ Littmann® Cardiology IV™	6181	FDA UDI	Class I	Active
3M™ Micropore™	1535-0	FDA UDI	Class I	Active
Bair Hugger™	52200	FDA UDI	Class II	Active
Filtek™	6028CT	FDA UDI	Class II	Active
3m™ Espe™	940642	FDA UDI	Class I	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.