ANVISA registration 80005430799Valid until Jun 23, 2035Glenoid component for shoulder arthroplasty
ANVISA Registration Number: 80005430799STRYKER DO BRASIL LTDATORNIER INCRisk Class IV
Device names
- Technical name
- Glenoid component for shoulder arthroplasty
- Commercial name
- TORNIER PERFORM REVERSED E AUGMENTED GLENOID SYSTEM
- Risk class
- Class IV
PT: Componente glenóideo para artroplastia de ombro
Registration details
- Registration Number
- 80005430799
- Process Number
- 25351397689202419
- CNPJ
- 02966317000102
Company information
- Registration Holder
- STRYKER DO BRASIL LTDA
- Manufacturer
- TORNIER INC
- Manufacturing Country
- United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
- Publication Date
- Jun 23, 2025
- Validity
- 23/06/2035
- Last Updated
- 08/18/2026 19:00:00
About this record
Access comprehensive regulatory information for Glenoid component for shoulder arthroplasty in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80005430799 and manufactured by TORNIER INC. The registration is held by STRYKER DO BRASIL LTDA with validity until Jun 23, 2035.
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