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 8 of 70

Device	Model / Reference	Registries	Class	Status
3M™ Littmann® Classic III™	5623	FDA UDI	Class I	Active
3m™	2181	FDA UDI	Class I	Active
Steri-Drape™	1094	FDA UDI	Class II	Active
3M™ Tegaderm™	1668	FDA UDI	Class I	Active
3M™ Clinpro™	7220SP	FDA UDI	Class II	Active
Bair Hugger™	77533	FDA UDI	Class II	Active
3M Company	2958	FDA UDI	Class I	Active
3M™ ESPE™ MDI One Piece Implant Tapered Abutment	2.9 mm x10 mm	FDA UDI	Class II	Unknown
3m™ Espe™	940646	FDA UDI	Class I	Active
3M™ Littmann®	6238	FDA UDI	Class I	Active
3m™ Espe™	801203	FDA UDI	Class I	Active
3M™ ESPE™ Iso-Form™	U-68	FDA UDI	Class I	Active
Imprint™	10971J	FDA UDI	Class II	Active
3M™ Red Dot™	2244	FDA UDI	Class II	Active
3M™ Unitek™	900244	FDA UDI	Class I	Active
Bair Hugger™	87500	FDA UDI	Class II	Active
3m™ Espe™	940514	FDA UDI	Class I	Active
Vitremer™	3303MP PEDO	FDA UDI	Class II	Active
3M™ ESPE™ MDI O-Ball Prosthetic Head	1.8 mm x 10 mm	FDA UDI	Class II	Unknown
3M™ Unitek™	900443	FDA UDI	Class I	Active
Futuro™	71057EN	FDA UDI	Class II	Active
Steri-Drape™	9077	FDA UDI	Class II	Active
3M™ Littmann®	2113	FDA UDI	Class I	Active
3M™ Medipore™	2860S-6U	FDA UDI	Class I	Active
3M™ Precise™	DS-15	FDA UDI	Class I	Active
3m™	6550B1	FDA UDI	Class II	Active
3M™ Unitek™	900245	FDA UDI	Class I	Active
3m™	1835FS	FDA UDI	Class II	Active
Filtek™	6029WD	FDA UDI	Class II	Active
3M™ Littmann® Cardiology IV™	6205	FDA UDI	Class I	Active
3M™ Littmann®	2119	FDA UDI	Class I	Active
3M™ Littmann® Master Classic II™	2630	FDA UDI	Class I	Active
Vitremer™	3303BLUE	FDA UDI	Class II	Active
3M™ Tegaderm™	3591	FDA UDI	Class I	Active
3M™ Bair Hugger™	67533	FDA UDI	Class II	Active
3M™ Coban™	2086S	FDA UDI	Class I	Active
3M™ Microfoam™	1528-4	FDA UDI	Class I	Active
Lava™	2614TN	FDA UDI	Class II	Unknown
3M™ Steri-Drape™ Pouch with Ioban™	6697	FDA UDI	Class II	Active
3M™ Steri-Strip™	B1551	FDA UDI	Class I	Active
3M™ Littmann®	5648	FDA UDI	Class I	Active
3m™	1860	FDA UDI	Class II	Active
3M™ Littmann®	2306	FDA UDI	Class I	Active
Steri-Drape™	9007A	FDA UDI	Class II	Active
Tegaderm™	77-2100K03	FDA UDI	U	Active
Comply™	1228	FDA UDI	Class II	Active
Steri-Drape™	7966	FDA UDI	Class II	Active
Steri-Drape™	1080P	FDA UDI	Class II	Active
3M™ ACE™ Brand	909001	FDA UDI	Class I	Active
Bair Paws™	81201	FDA UDI	Class II	Unknown

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.