1,381 results · 19ms · Sources: EU EUDAMED, US FDA

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HEMOCHRON TEST TUBE

FDA Adverse Event
Malfunction ·INTL TECHNIDYNE CORP.·Product code JBT·October 30, 1995

HEMOCHRON JR.

FDA Adverse Event
Injury ·INTERNATION TECHNIDYNE CORP.·Product code JBT·November 6, 1995

UNKNOWN HIP FEMORAL CONSTRUCT RECLAIM

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LZO·July 30, 2024

UNK HIP FEMORAL STEM RECLAIM PROXIMAL BODY

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code LPH·July 31, 2024

UNK HIP FEMORAL STEM RECLAIM DISTAL STEM

FDA Adverse Event
Injury ·DEPUY IRELAND - 9616671·Product code LPH·July 31, 2024

RUNTHROUGH NS

FDA Adverse Event
Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·April 8, 2025

Timer, Coagulation

FDA classification
FDA Class 2 ·Timer, Coagulation

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

FDA Enforcement
Class I ·Ongoing·Baxter Healthcare Corporation·May 21, 2025

Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.

FDA Enforcement
Class I ·Ongoing·Baxter Healthcare Corporation·May 21, 2025

Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A, 3) BT-20-0002AP, 4) BT-20-0007, 5) BT-20-0011, and 6) RMS010118CP

FDA Enforcement
Class I ·Ongoing·Baxter Healthcare Corporation·October 30, 2024

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

FDA Recall
Open, Classified ·Baxter Healthcare Corporation·Product code CBK·April 7, 2025

Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.

FDA Recall
Open, Classified ·Baxter Healthcare Corporation·Product code CBK·April 7, 2025

Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A, 3) BT-20-0002AP, 4) BT-20-0007, 5) BT-20-0011, and 6) RMS010118CP

FDA Recall
Open, Classified ·Baxter Healthcare Corporation·Product code CBK·September 12, 2024

JBC CORP

FDA registration
JBC CORP·5 products·🇺🇸 United States

IBT Scientific

FDA registration
IBT Scientific·5 products·🇺🇸 United States

JBC AND COMPANY

FDA registration
JBC AND COMPANY·1 product·🇺🇸 United States

JBC TECHNOLOGIES, INC.

FDA registration
JBC TECHNOLOGIES, INC.·1 product·🇺🇸 United States

JBC TECHNOLOGIES, INC.

FDA registration
JBC TECHNOLOGIES, INC.·1 product·🇺🇸 United States

Lunit INSIGHT DBT

FDA UDI
Lunit Inc.·08800076000148·

Lunit INSIGHT DBT

FDA UDI
Lunit Inc.·08800076000162·