CENTRO DE CELULAS MADRE Y BIOTECNOLOGIA S.A.S.
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.
コロンビアの医療およびヘルスケア製品のメーカー。
セントロ・デ・セルラス・マドレ・イ・バイオテクノロジー社 S.A.S.コロンビアのペレイラで医療およびヘルスケア製品を製造しています。同社はアクティブな企業 Web サイトを維持し、企業または機関バイヤーにサービスを提供しています。
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Pereira, Colombia
- Founded
- 2014 (from our catalogue record; not confirmed by the company or by a state register)
- Website
- https://www.regencord.com
- Categories
- 医療およびヘルスケア用品
- Markets
- コロンビア
What is established and what is not
No researcher review has been written for this company yet. 4 official records from 1 official source are on file. 4 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. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-08-09. Mail server of the company domain
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-09. Domain registry record
- 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. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-09. 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. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-09. OpenSanctions
- Registry ID checks out with the state register (record type: registry-id-verified) [official record; status amber] Helps confirm the company on this page is the same legal entity as in the register. checked 2026-08-16. RUES, Registro Único Empresarial y Social (Confecámaras)
- On the company register (record type: registered-since) [official record; status amber] Shows how long the company has been on the state register, which is hard to fake and easy to check. checked 2026-08-16. RUES, Registro Único Empresarial y Social (Confecámaras)
- Directors named in the company register (record type: leadership-on-record) [official record; status green] The people leading the company are named in a public record. checked 2026-08-16. RUES, Registro Único Empresarial y Social (Confecámaras)
- registry-activity (record type: registry-activity) [official record; status green] Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-08-16. RUES, Registro Único Empresarial y Social (Confecámaras)
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)
Check independently
Before a first order, ask for the production site address and a document linking that site to this legal entity.