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Data / Medical devices / Japan / Me Center Of Terumo Corp.

Me Center Of Terumo Corp.: FDA-registered device maker in FUJINOMIYA Shizuoka, Japan, 1 510(k) clearance

Me Center Of Terumo Corp. is registered with the FDA (registration 9681837) in FUJINOMIYA Shizuoka, Japan. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 27, 1985. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9681837
FEI number
3003753439
Address
150 Maimaigi-Cho, FUJINOMIYA Shizuoka, Japan, 418-0015
Owner or operator
TERUMO CORP. (8010026)
Roles
Manufacturer
First device listed
November 29, 2007
Registered through
2026
Brand names listed
CAPIOX Luer Thermistor, CAPIOX Luer Thermistor Wire Blue Cable (ME Center), CAPIOX Luer Thermistor Wire Red Cable (ME Center)

Devices it lists

DeviceProduct codeClassRoleSource
Continuous Measurement ThermometerFLL2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 27, 1985K852087CAPIOX LUER DESIGN THERMISTORS & CAPIOX CONNECTORSFLLSubstantially EquivalentTerumo Medical Corp.accessdata.fda.gov

Compare with other makers

Updated June 27, 1985. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.