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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 11 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Durapore™	1538-3D	FDA UDI	Class I	Active
3M™ Unitek™	900114	FDA UDI	Class I	Active
3m™	1919F	FDA UDI	Class I	Active
3M™ Tegaderm™	90024	FDA UDI	Class I	Active
3M™ Tegaderm™	9124	FDA UDI	U	Active
Steri-Drape™	1008	FDA UDI	Class II	Unknown
Lava™	2614A1-LT	FDA UDI	Class II	Active
3m™	1840	FDA UDI	Class II	Active
Bair Hugger™	84201	FDA UDI	Class II	Active
3M™ Aura™	1870+	FDA UDI	Class II	Active
3m™ Espe™	DLR5	FDA UDI	Class I	Active
Futuro™	71061EN	FDA UDI	Class II	Active
Steri-Drape™ Ioban™ 2	6697CA	FDA UDI	Class II	Active
3M™ Nexcare™	576-30PB	FDA UDI	Class I	Active
3M™ Red Dot™	2570	FDA UDI	Class II	Active
Comply™	00135LF	FDA UDI	Class II	Active
3M™ Steri-Drape™ Cesarean-Section Drape with Ioban™	6697CA	FDA UDI	Class II	Active
Steri-Drape™	9009	FDA UDI	Class II	Active
Futuro™	71045EN	FDA UDI	Class II	Active
3m™ Espe™	940333	FDA UDI	Class I	Active
3m™ Espe™	DLR3	FDA UDI	Class I	Active
3m™ Espe™	940631	FDA UDI	Class I	Active
3m™ Espe™	ELR7	FDA UDI	Class I	Active
Paradigm™	5312	FDA UDI	Class II	Active
Filtek™	4867B1	FDA UDI	Class II	Active
Steri-Drape™	1030	FDA UDI	Class II	Active
Nova Plus®	V2228-5	FDA UDI	Class II	Active
Lava™	1334D2-LT	FDA UDI	Class II	Unknown
3M™ Tegaderm™	3593	FDA UDI	Class I	Active
3m™ Espe™	940644	FDA UDI	Class I	Active
Filtek™	6032D2	FDA UDI	Class II	Active
Filtek™	6032A2-S	FDA UDI	Class II	Active
Bair Hugger™ Novaplus™	42234	FDA UDI	Class II	Active
3M Company	2956	FDA UDI	Class I	Active
3m™ Espe™	14	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	L-65	FDA UDI	Class I	Active
3M™ Tegaderm™	1839-2100	FDA UDI	Class I	Active
3M™ Bair Hugger™	67500	FDA UDI	Class II	Active
Lava™	2912BL-LT	FDA UDI	Class II	Active
Filtek™	6033A3.5	FDA UDI	Class II	Unknown
Ioban™ 2	6651EZ	FDA UDI	Class II	Active
Ranger™	24750	FDA UDI	Class II	Active
3M™ Nexcare™	781-1PK	FDA UDI	Class I	Active
3m™	MS03	FDA UDI	Class I	Active
Curos™	CSVI-270	FDA UDI	U	Active
Z100™	5906UD	FDA UDI	Class II	Active
3M™ Unitek™ Temporary Anchorage Device (TAD)	10 mm	FDA UDI	Class II	Active
Bair Hugger™	83101	FDA UDI	Class II	Active
3m™ Espe™	36	FDA UDI	Class I	Active
Filtek™	6032A1	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.