Stericycle
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.
医療廃棄物 |臨床廃棄物の処理 |ステリスクリ
業界をリードする当社の医療、鋭利物、医薬品廃棄物の処理およびコンプライアンス トレーニング ソリューションについて学び、組織に最適なものを見つけてください。
- 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
- County Dublin, Ireland
- Website
- https://stericycle.ie
- Categories
- 医薬品製造, 医療およびヘルスケア用品
What is established and what is not
No researcher review has been written for this company yet. No fact of any kind is on file either. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
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)
Goods family established: 医療およびヘルスケア用品 (the company's own text). The exact product, operation and trade route needed to determine a product-specific requirement are not established here. Product-specific import rules not established for the catalog category 医薬品製造: no record or company text names goods of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.