Symatese Aesthetics Ltd.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
ANVISA, cơ quan quản lý y tế Brazil, có chứng chỉ Thực hành Sản xuất Tốt hợp lệ cho nhà máy này, bao gồm các thiết bị y tế, có hiệu lực đến ngày 27 tháng 1 năm 2027. Giấy chứng nhận được cấp sau khi kiểm tra chính nhà máy, đó là lý do tại sao cơ quan quản lý nước ngoài đặt tên cho địa điểm này: hàng hóa sản xuất tại đây được phép lưu hành trên thị trường Brazil. Giấy chứng nhận ghi địa chỉ địa điểm là TẦNG 1, KHỐI GIAI ĐOẠN 2, TÒA NHÀ CÔNG NGHIỆP BPML - LA CLEMENCE - RIVIERE DU REMPART, 31105 REPÚBLICA DE MAURÍCIO. Số quy trình 25351242002201933.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Riviere Du Rempart, Mauritius
- Categories
- Vật tư y tế và chăm sóc sức khỏe
- Markets
- Mauritius, Brazil
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 3 official records from 3 official sources are on file. 2 other entries are not official records: our own technical checks and searches, open directory listings, our inferences or the company's own statements. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. checked 2026-09-02. OpenSanctions
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. checked 2026-09-02. OpenSanctions
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status green] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-08-21. List of VAT Registered Persons (MRA, Mauritius)
- manufacturing-practice-certified (record type: manufacturing-practice-certified) [official record; status green] A regulator of health products inspected this site and certified how it manufactures the product class named, for example medical devices or cosmetics. It is about manufacturing practice at the site, not a medicines licence. checked 2026-10-03. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- Active taxpayer registration (record type: tax-filing-active) [official record; status green] Registered as an active taxpayer. checked 2026-10-03. Mauritius Revenue Authority (MRA), List of VAT Registered Persons
Relationships
1 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Recorded in a source
- 1ST FLOOR, PHASE 2 BLOCK, BPML INDUSTRIAL BUILDING - LA CLEMENCE - RIVIERE DU REMPART, 31105 REPÚBLICA DE MAURÍCIO: Manufactures at the site. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)