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Micromedics, Inc.

United States·US-MF-000018365

Last updated September 17, 2026

Information

Country: United States
Address: 1270, Eagan Industrial Road , St. Paul, United States
Website: nordsonmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1 651.236.7869
PRRC Contact: Nicole Freeberg
EUDAMED SRN: US-MF-000018365
FDA FEI Number: 2183425
DUNS Number: 066839630

Catalogue (231)

Page 5 of 5

Device	Model / Reference	Registries	Class	Status
FibriJet	SA-3651	EUDAMED	Class IIa	Active
OsteoPrecision Graft Delivery Device	GD-1015-150	EUDAMEDFDA UDI	Class IIa	Active
FibriJet Regulator	SA-6030	EUDAMEDFDA UDI	Class IIa	Active
OsteoPrecision	GD-1215-150	EUDAMED	Class IIa	Active
DuploTip	SA376003006666	EUDAMED	Class IIa	Active
Baxter Endoscopic Applicator	0600125	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-4400	EUDAMEDFDA UDI	Class IIa	Active
Biomet Biologics	800-0207	EUDAMED	Class IIa	Active
360° Endoscopic Applicator	SA-3768	EUDAMEDFDA UDI	Class IIa	Active
Biomet Biologics	800-0260	EUDAMED	Class IIa	Active
Arthrex Applicator With Mixer and Spray Tip Kit	ABS-10052	EUDAMED	Class IIa	Active
Arthrex Applicator	ABS-10052	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3649	EUDAMED	Class IIa	Active
DuploTip	SA375003005555	EUDAMEDFDA UDI	Class IIa	Active
OsteoPrecision Graft Delivery Device	GD-1015-050	EUDAMED	Class IIa	Active
FibriJet	800-0251	EUDAMEDFDA 510(k)FDA UDI	Class IIa	Active
FibriJet	SA-3671-100	EUDAMEDFDA UDI	Class IIa	Active
Biomet Biologics	800-0252	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3674	EUDAMEDFDA UDI	Class IIa	Active
DuploTip	0601138	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-1060	EUDAMEDFDA UDI	Class IIa	Active
DuploTip	0601138	EUDAMED	Class IIa	Active
DuploSpray MIS	0600044	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3671	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-1060	EUDAMED	Class IIa	Active
FibriJet	SA-3673	EUDAMED	Class IIa	Active
360° Endoscopic Applicator	SA-3768	EUDAMED	Class IIa	Active
Biomet Biologics	800-0260	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3667	EUDAMED	Class IIa	Active
Biomet Biologics	800-0202	EUDAMED	Class IIa	Active
DuploSpray MIS	0600043	EUDAMEDFDA UDI	Class IIa	Active

Related Companies

Authorised Representatives

MDSS GmbH DE

Importers

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Notified Bodies

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Authorities

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FDA Recalls (5)

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
Oct 20, 2016	Z-1817-2017	—	terminated	The sterile packaging may contain small channels in the seal of the pouch, If the channels are present, the package integrity may be compromised which may affect sterility assurance.
Mar 15, 2010	Z-0347-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.
Mar 15, 2010	Z-0348-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.
Mar 15, 2010	Z-0346-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches potentially resulting in a non-sterile product which may cause transmission of disease or infection.
Mar 15, 2010	Z-0345-2011	—	terminated	Micromedics, Inc is conducting a product recall on a number of medical device products because of weak seals of the sterile pouches, potentially resulting in a non-sterile product which may cause transmission of disease or infection.