Dipped Products
Producent rękawic z naturalnego kauczuku w Kolombo, spółka zależna Hayleys, produkująca ponad 2 miliardy rękawiczek rocznie.
Dipped Products to największy producent rękawic gumowych na Sri Lance, spółka zależna Hayleys Group. Założona w 1976 roku firma produkuje rękawice medyczne, przemysłowe i domowe w swoich czterech fabrykach na Sri Lance i Tajlandii, eksportując ponad 2 miliardy rękawiczek rocznie.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Colombo, Sri Lanka
- Founded
- 1976
- Website
- dippedproducts.com
- Categories
- Artykuły medyczne i związane z opieką zdrowotną, Dostawy przemysłowe, Produkty gumowe i kompozytowe
- Markets
- Stany Zjednoczone, Niemcy, Wielka Brytania, Australia
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-08 Domain registry record
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
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)
- Chemical substances imported into the EU above 1 tonne/year must be REACH-registered. ECHA (REACH)