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Anti-Embolism Stocking - ANVISA Registration 81356112302

Access comprehensive regulatory information for Anti-Embolism Stocking in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81356112302 and manufactured by COVIDIEN llC. The registration is held by CARDINAL HEALTH DO BRASIL LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for 4 related devices, regulatory compliance details, 5 companies making the same product including TEXPON S.A, BSN MEDICAL INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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81356112302
4 Related Devices
Registration Details
ANVISA Registration Number: 81356112302
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Related Devices (4)

MEIA ANTI-EMBOLISMO T.E.D. KENDALL
Risk Class I

Registration Details

81356112302

25351552101201840

19585158000107

Company Information

COVIDIEN llC
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 03, 2018

VIGENTE

09/18/2025 19:00:01

MEIA ANTI-EMBOLISMO T.E.D. KENDALL
Risk Class I

Registration Details

81356112302

25351552101201840

19585158000107

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 03, 2018

VIGENTE

09/18/2025 19:00:01

MEIA ANTI-EMBOLISMO T.E.D. KENDALL
Risk Class I

Registration Details

81356112302

25351552101201840

19585158000107

Company Information

United Kingdom
PT: REINO UNIDO

Dates and Status

Sep 03, 2018

VIGENTE

09/18/2025 19:00:01

MEIA ANTI-EMBOLISMO T.E.D. KENDALL
Risk Class I

Registration Details

81356112302

25351552101201840

19585158000107

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 03, 2018

VIGENTE

09/18/2025 19:00:01