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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 4 of 5

Device	Model / Reference	Registries	Class	Status
FibriJet	SA-3670	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3660	EUDAMEDFDA UDI	Class IIa	Active
DuploTip	SA374003004444	EUDAMED	Class IIa	Active
DuploSpray MIS	0600134	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3303	EUDAMEDFDA UDI	Class IIa	Active
Biomet Biologics	800-0250	EUDAMEDFDA UDI	Class IIa	Active
OsteoPrecision Graft Delivery Device	GD-1015-150	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3675	EUDAMEDFDA UDI	Class IIa	Active
Arthrex BioXpress	ABS-10053-15	EUDAMED	Class IIa	Active
Biomet Biologics	800-0252	EUDAMED	Class IIa	Active
FibriJet	SA-3303	EUDAMED	Class IIa	Active
DuploTip	SA376003006666	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3678	EUDAMEDFDA UDI	Class IIa	Active
DuploTip	0601137	EUDAMEDFDA UDI	Class IIa	Active
Magellan Dispenser Tip	AMS700	EUDAMED	Class IIa	Active
Biomet Rigid Endoscopic Tip	800-0208	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3651	EUDAMEDFDA UDI	Class IIa	Active
A020199	LS-1015-150	EUDAMED	Class IIa	Active
Exactech Accelerate	620-00-02	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-1001	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3667	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3647	EUDAMEDFDA UDI	Class IIa	Active
DuploSpray	0600030	EUDAMEDFDA UDI	Class IIa	Active
Arthrex BioXpress	ABS-10053-10	EUDAMED	Class IIa	Active
Baxter Gasless Tip Applicator	601156	EUDAMEDFDA UDI	Class IIa	Active
Arthrex BioXpress	ABS-10053-15-45	EUDAMEDFDA UDI	Class IIa	Active
Arthrex BioXpress	ABS-10053-10-45	EUDAMEDFDA UDI	Class IIa	Active
Spray Set 360 Endoscopic Applicator with Snap Lock	SA3768111	EUDAMEDFDA UDI	Class IIa	Active
Biomet Biologics	800-0207	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3305	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3649	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	800-0251	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3310	EUDAMEDFDA UDI	Class IIa	Active
FibriJet Regulator	SA-6030	EUDAMED	Class IIa	Active
FibriJet	SA-3673	EUDAMEDFDA UDI	Class IIa	Active
DuploSpray MIS	0600029	EUDAMEDFDA UDI	Class IIa	Active
DuploSpray	0600030	EUDAMED	Class IIa	Active
Baxter Gasless Tip Applicator	601156	EUDAMEDFDA UDI	Class IIa	Active
Baxter Gasless Tip	601158	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3620	EUDAMEDFDA UDI	Class IIa	Active
Spray Set 360 Endoscopic Applicator with Snap Lock	SA3768111	EUDAMED	Class IIa	Active
LifeSpine	LS-1015-150	EUDAMED	Class IIa	Active
DuploSpray MIS	0600033	EUDAMEDFDA UDI	Class IIa	Active
Magellan Dispenser Tip	AMS612	EUDAMEDFDA UDI	Class IIa	Active
FibriJet	SA-3675	EUDAMED	Class IIa	Active
OsteoPrecision	GD-1115-150	EUDAMEDFDA UDI	Class IIa	Active
Baxter Gasless Replacement Tips	601160	EUDAMEDFDA UDI	Class IIa	Active
Arthrex BioXpress	ABS-10053-10	EUDAMED	Class IIa	Active
Magellan Dispenser Tip	AMS700	EUDAMED	Class IIa	Active
FibriJet	SA-3618	EUDAMEDFDA UDI	Class IIa	Active

Related Companies

Authorised Representatives

MDSS GmbH DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.