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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 18 of 70

Device	Model / Reference	Registries	Class	Status
Tegaderm™	1665	FDA UDI	U	Active
Steri-Drape™	9000A	FDA UDI	Class II	Active
Filtek™	4720B2	FDA UDI	Class II	Active
Steri-Drape™	1018L	FDA UDI	Class II	Active
3M™ Micropore™	1530-154	FDA UDI	Class I	Active
3M™ Tegaderm™	91111	FDA UDI	Class I	Unknown
3M™ Cavilon™	5051	FDA UDI	Class I	Active
RelyX™	2721	FDA UDI	Class II	Active
3m™ Espe™	37	FDA UDI	Class I	Active
3M™ ESPE™ Protemp™	50616	FDA UDI	Class I	Active
Steri-Drape™	9016	FDA UDI	Class II	Active
Paradigm™	2714A1-S	FDA UDI	Class II	Active
Steri-Drape™	9084	FDA UDI	Class II	Active
Filtek™	6021A1	FDA UDI	Class II	Active
3m™ Espe™	914003	FDA UDI	Class I	Active
Steri-Drape™	7964	FDA UDI	Class II	Active
3M™ Unitek™	900342	FDA UDI	Class I	Active
Steri-Drape™	9054	FDA UDI	Class II	Active
3m™ Espe™	2	FDA UDI	Class I	Active
3M™ Littmann® Master Cardiology™	2178	FDA UDI	Class I	Active
Bair Hugger™	81501	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	U-77	FDA UDI	Class I	Active
Steri-Drape™	1024	FDA UDI	Class II	Active
3M™ Littmann® Classic III™	5812	FDA UDI	Class I	Active
3M™ Unitek™ Temporary Anchorage Device (TAD)	6 mm	FDA UDI	Class II	Active
3M™ Littmann®	8574	FDA UDI	Class II	Active
Bair Paws™	89500	FDA UDI	Class II	Unknown
3M™ Bair Hugger™	69500	FDA UDI	Class II	Active
3m™	75030	FDA UDI	Class II	Active
3M™ Cavilon™	3346NP	FDA UDI	Class I	Active
3M™ Littmann® Classic III™	5811	FDA UDI	Class I	Active
3M™ Filtek™	6032W	FDA UDI	Class II	Active
Adper™ Scotchbond™	7545S	FDA UDI	Class II	Unknown
3M™ Littmann® Classic III™	5864	FDA UDI	Class I	Active
Futuro™	71033OTHEN	FDA UDI	Class II	Active
3m™ Espe™	940313	FDA UDI	Class I	Active
3M™ Microfoam™	1528-2	FDA UDI	Class I	Active
3M™ Medipore™	2968	FDA UDI	Class I	Active
3M™ Littmann®	8869	FDA UDI	Class II	Active
Filtek™	6033A4	FDA UDI	Class II	Unknown
3m™ Espe™	2921	FDA UDI	Class I	Unknown
3M™ Medipore™	2864S	FDA UDI	Class I	Active
3M™ Unitek™	902600	FDA UDI	Class I	Active
Futuro™	71073EN	FDA UDI	Class II	Active
3M™ ESPE™ Iso-Form™	L-40	FDA UDI	Class I	Active
3M™ Cavilon™	3343E	FDA UDI	Class I	Active
Imprint™	10971	FDA UDI	Class II	Active
3M™ Tegaderm™	1882NS	FDA UDI	Class I	Active
Z100™	5904A2	FDA UDI	Class II	Active
Z100™	5906P	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.