International safety notice
CHAIRS, EXAMINATION/TREATMENT [] Electric Chairs, Disabled Patients,, Geratric, Pediatric, Lifting, Dentistry, Ophthalmology, Otorhinolaryngology, Pediatrics, Podiatrics, Mammography, Convalescence, Transfer, Fluoroscopy
Brazil / Anvisa · BRA · Nov 3, 2000
Key facts
| Title | CHAIRS, EXAMINATION/TREATMENT [] Electric Chairs, Disabled Patients, , Geratric, Pediatric, Lifting, Dentistry, Ophthalmology, Otorhinolaryngology, Pediatrics, Podiatrics, Mammography, Convalescence, Transfer, Fluoroscopy |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Electric Reclining Chairs for CHAIRS, EXAMINATION/TREATMENT [16-437] Chairs, Disabled Patient [18-406] Chairs, Disabled Patient, Geriatric [10-796] Chairs, Disabled Patient, Pediatric [10-797] Chairs, Disabled Patient, Seat-Lifting [17-975] Chairs, Examination/Treatment, Dentistry [10-792] Chairs, Examination/Treatment, Ophthalmology [15-723] Chairs, Examination/Treatment, Otorhinolaryngology [10-794] Chairs, Examination/Treatment, Pediatrics [16-169] Chairs, Examination/Treatment, Podiatry [10-799] Chairs, Flotation Therapy [10-795] Chairs, Mammography [18-402] Chairs, Patient Recovery [18-404] Chairs, Patient Transfer [16-639] Chairs, Patient Transfer, Stair [16-906] Chairs, Radiography/Fluoroscopy [16-673] Chairs, Radiography/Fluoroscopy, Head [18-400] Chairs, Radiography/Fluoroscopy, Head/Torso [18-401], |
| Models | 18-400, 18-401, 16-437, 10-797, 16-169, 15-723, 17-975, 10-792, 10-796, 10-795, 16-639, 18-404 and 6 more |
| Date | Nov 3, 2000 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1