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MERCEDES MEDICAL LLC

US

Last updated September 17, 2026

Information

Country
US
Address
12210 Rangeland Parkway, Lakewood Ranch, FL, 34211
Website
—
LinkedIn
—
Facebook
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Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
1000442352
DUNS Number
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Catalogue (32)

DeviceModel / ReferenceRegistriesClassStatus
BluWing MER 1921
FDA UDI
Class IIActive
Tanner Scientific® TNR DOA13A
FDA UDI
Class IIActive
Platinum+ MER MMDOAY6125
FDA UDI
Class IIActive
Tanner Scientific® TNR IFOB
FDA UDI
Class IIActive
BluTouch TNR 700S
FDA UDI
Class IActive
BluRapids™ TNR CDOA262
FDA UDI
Class IIActive
BluRapids™ TNR CDOA7125A3
FDA UDI
Class IIActive
BluTouch TNR 700M
FDA UDI
Class IActive
BluWing MER 1923
FDA UDI
Class IIActive
Vacuflow™ MED 5021
FDA UDI
Class IIActive
Tanner Scientific® TNR IFOB36
FDA UDI
Class IIActive
Vacuflow™ MED 5025
FDA UDI
Class IIActive
Vacuflow™ MED 5023
FDA UDI
Class IIActive
Tanner Scientific® TNR HCGCOMBO
FDA UDI
Class IIActive
BluRapids™ TNR CDOA261
FDA UDI
Class IIActive
Vacuflow™ MED 5223
FDA UDI
Class IIActive
Tanner Scientific® TNR 10SG
FDA UDI
Class IActive
BluRapids™ TNR CDOA7125
FDA UDI
Class IIActive
Vacuflow™ MED 5225
FDA UDI
Class IIActive
BluRapids™ TNR CDOA5125A3
FDA UDI
Class IIActive
BluRapids™ TNR MM5CPCP
FDA UDI
Class IIActive
BluWing MER 1925
FDA UDI
Class IIActive
BluRapids™ TNR CDOA2135
FDA UDI
Class IIActive
Tanner Scientific® TNR DOA12A
FDA UDI
Class IIActive
Vacuflow™ MED 5221
FDA UDI
Class IIActive
BluTouch TNR 700L
FDA UDI
Class IActive
BluRapids TNR CDOA6125M
FDA UDI
Class IIActive
BluRapids™ TNR CDOA6125
FDA UDI
Class IIActive
BluTouch TNR 700XL
FDA UDI
Class IActive
Platinum+ MER HCDOAY6125
FDA UDI
Class IIActive
BluRapids™ TNR MM5CMET
FDA UDI
Class IIActive
BluRapids™ TNR MMC12MOP
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

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.

DateRecall No.ClassStatusReason
Jun 10, 2021Z-2066-2021—terminated

No 510(k) clearance

Jun 10, 2021Z-2067-2021—terminated

No 510(k) clearance