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InBody Co., Ltd. devices, product family

by InBody Co., Ltd. 12 variants Basic UDI-DI 880920959F2YB

Shared by every variant

Manufacturer
InBody Co., Ltd.(12)
Basic UDI-DI
880920959F2YB
Risk class
Class IIa
Legislation
MDR
EMDN category
NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGESDYNAMOMETRIC SYSTEMS FOR MOVEMENT ANALYSIS – OTHER
Market status
11 on the market1 not intended for the eu market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 880920959F2YB.

Certificates

1 certificate naming this Basic UDI-DI · EUDAMED

  • KR23/00000132 Quality management system · refdata.applicable-legislation.mdr supplemented
    Notified body 1639 · holder InBody Co., Ltd. · issued 3 Jun 2024 · expires 9 Aug 2028

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 12 devices listed on this page; other pages of the family can carry others.

Variants

12 devices · page 1 of 1

Variants of InBody Co., Ltd. devices, Basic UDI-DI 880920959F2YB
UDI-DISize and differences
BPBIO320 B8 / BPBIO32008809209592222 —On the market
BPBIO320 B8 / BPBIO32008809209590723 —On the market
BPBIO320 B8 / BPBIO32008809209590716 —On the market
BPBIO320n E4 / BPBIO32008809209591140 —On the market
BPBIO320n E4 / BPBIO32008809209591157 —Not intended for the EU market
BPBIO320n E4 / BPBIO32008809209591164 —On the market
BPBIO320S E5 / BPBIO32008809209590839 —On the market
BPBIO320S E5 / BPBIO32008809209592215 —On the market
BPBIO320S E5 / BPBIO32008809209590686 —On the market
BPBIO330 82 / BPBIO32008809209591119 —On the market
BPBIO330n H4 / BPBIO32008809209591195 —On the market
BPBIO330S F2 / BPBIO32008809209591713 —On the market