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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 58 of 70

Device	Model / Reference	Registries	Class	Status
Filtek™	4720C2	FDA UDI	Class II	Active
Steri-Drape™	2040	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6179	FDA UDI	Class I	Active
Bair Hugger™	42568	FDA UDI	Class II	Active
Z100™	5905A1	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6164	FDA UDI	Class I	Active
Steri-Drape™	9042	FDA UDI	Class II	Active
Nova Plus®	V2560	FDA UDI	Class II	Active
3m™ Espe™	EUR7	FDA UDI	Class I	Active
3M™ Clinpro™	12626T	FDA UDI	Class II	Active
3M™ Unitek™	900215	FDA UDI	Class I	Active
Lava™	2912B1-HT	FDA UDI	Class II	Active
3m™ Espe™	77580	FDA UDI	Class II	Active
3M™ Steri-Drape™	9097	FDA UDI	Class II	Active
3M™ Unitek™	900314	FDA UDI	Class I	Active
3m™ Espe™	942501	FDA UDI	Class I	Active
Filtek™	4720A3	FDA UDI	Class II	Active
3M™ Littmann® Classic II™	2201	FDA UDI	Class I	Active
Paradigm™	2710A1-S	FDA UDI	Class II	Unknown
3M™ Durapore™	1590S-1	FDA UDI	Class I	Active
Steri-Drape™	9019	FDA UDI	Class II	Active
3M™ ESPE™ MDI Standard O-Ball and Collar	1.8 mm x 15 mm	FDA UDI	Class II	Unknown
3M™ Unitek™	907033	FDA UDI	Class I	Active
3M™ Cavilon™	3343E	FDA UDI	Class I	Active
3M™ Littmann®	5811	FDA UDI	Class I	Active
Steri-Drape™	9196P	FDA UDI	Class II	Active
Ioban™ 2	6661EZ	FDA UDI	Class II	Active
Steri-Drape™	1022	FDA UDI	Class II	Active
3M™ Bair Hugger™	53700	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6169	FDA UDI	Class I	Active
Lava™	2012D2-LT	FDA UDI	Class II	Active
Bair Paws™	83001	FDA UDI	Class II	Unknown
3M™ Tegaderm™	90004	FDA UDI	Class I	Active
Filtek™	6033D2	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-46	FDA UDI	Class I	Active
Bair Hugger™	84003	FDA UDI	Class II	Active
3m™ Espe™	44	FDA UDI	Class I	Active
Filtek™	6021A4	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-53	FDA UDI	Class I	Active
3M™ Durapore™	1591-2	FDA UDI	Class I	Active
Steri-Drape™	9043	FDA UDI	Class II	Active
Lava™	2614A3-HT	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6154	FDA UDI	Class I	Active
Filtek™	6033A2-S	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-45	FDA UDI	Class I	Active
3M™ Tegaderm™	90640	FDA UDI	Class I	Active
3M™ Littmann®	8480	FDA UDI	Class II	Active
3M™ Littmann®	5803	FDA UDI	Class I	Active
3m™ Espe™	EUL2	FDA UDI	Class I	Active
3m™ Espe™	ND-96	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.