Is this your brand? Sign in to claim ownership.

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 10 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Medipore™	2963	FDA UDI	Class I	Active
3m™ Espe™	11	FDA UDI	Class I	Active
3M™ Attest™	1492VS	FDA UDI	Class II	Active
Comply™ SteriGage™	1243B	FDA UDI	Class II	Active
Paradigm™	3714A3.5	FDA UDI	Class II	Active
3M™ Unitek™	900143	FDA UDI	Class I	Active
3M™ Nexcare™ Micropore™	530-P2	FDA UDI	Class I	Active
Filtek™	6029D2B	FDA UDI	Class II	Active
Steri-Drape™	1194P	FDA UDI	Class II	Active
Filtek™	6028A3D	FDA UDI	Class II	Active
CavityShield™	12143	FDA UDI	Class II	Unknown
3M™ ESPE™ Iso-Form™	L-73	FDA UDI	Class I	Active
3M™ Littmann®	5962	FDA UDI	Class I	Active
3M™ Littmann®	6152	FDA UDI	Class I	Active
3M™ ESPE™ MDI Standard Square Head and Collar	1.8 mm x 18 mm	FDA UDI	Class II	Unknown
3M™ Filtek™	6032A2-S	FDA UDI	Class II	Active
Steri-Drape™	9014	FDA UDI	Class II	Active
3m™ Espe™	6LR3	FDA UDI	Class I	Active
Lava™	5072A2-HT	FDA UDI	Class II	Active
Filtek™	6029XWE	FDA UDI	Class II	Active
3M™ Transpore™	1534-1	FDA UDI	Class I	Active
Steri-Drape™	1018	FDA UDI	Class II	Active
3M™ Reston™	2851H	FDA UDI	Class I	Active
3M™ Unitek™	900117	FDA UDI	Class I	Active
3m™ Espe™	940640	FDA UDI	Class I	Active
Tegaderm™	90305	FDA UDI	U	Active
3M™ Littmann®	2122	FDA UDI	Class I	Active
Bair Hugger™ Novaplus™	45534	FDA UDI	Class II	Active
3m™ Espe™	940535	FDA UDI	Class I	Active
Lava™	3112A3-LT	FDA UDI	Class II	Unknown
Ketac™	3304A3.5	FDA UDI	Class II	Active
3M™ Unitek™	900332	FDA UDI	Class I	Active
3m™	1860S	FDA UDI	Class II	Active
3M™ Filtek™	3700T27	FDA UDI	Class I	Active
Filtek™	6020D3	FDA UDI	Class II	Active
3M™ Unitek™	900142	FDA UDI	Class I	Active
3M™ Filtek™	3700T27	FDA UDI	Class I	Active
Steri-Drape™	1023	FDA UDI	Class II	Active
Tegaderm™	90303	FDA UDI	U	Active
Steri-Drape™	9053	FDA UDI	Class II	Active
3M™ Durapore™	1591-1	FDA UDI	Class I	Active
3M™ Transpore™	1534S-1	FDA UDI	Class I	Active
3M™ Medipore™	2860S-2U	FDA UDI	Class I	Active
3m™	SPS-YP1010	FDA UDI	Class I	Active
3M™ Cavilon™	3344E	FDA UDI	Class I	Active
3m™	1838FSG	FDA UDI	Class II	Active
Ranger™	24450	FDA UDI	Class II	Active
Clinpro™	12622	FDA UDI	Class II	Active
Steri-Drape™	9074	FDA UDI	Class II	Active
Nexcare™	H1820	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.