Dah Chong Hong
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.
Küresel tıbbi ürün ve gıda ürünleri ithal eden baskın dağıtım motoru
Soğuk zincir etlerinin, klinik ilaçların ve sağlık elektroniğinin büyük ölçekli ithalatını yönetiyoruz. Ağımız hastanelere, otellere ve büyük perakende satış noktalarına teslimat yapmaktadır.
- Type
- Not established by any record (our catalog import lists it as distributor; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Hong Kong
- Founded
- 1949 (matches the state register)
- Website
- dch.com.hk
- Categories
- Dondurulmuş ve Soğutulmuş Gıdalar, Özel ve Gurme Yiyecekler, Tıbbi ve Sağlık Malzemeleri
- Markets
- Çin Hong Kong ÖİB, Çin Makao ÖİB
What is established and what is not
No researcher review has been written for this company yet. 5 official records from 2 official sources are on file. 3 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
- 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 2026-08-05. OpenSanctions
- 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 2026-08-05. OpenSanctions
- 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 2026-08-05. Mail server of the company domain
- Legal entity ID lapsed (record type: lei-lapsed) [official record; status amber] The global finance identifier was not renewed. checked 2026-09-07. GLEIF global LEI register (golden copy)
- 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 2026-09-06. Hong Kong Companies Registry, live local companies (data.cr.gov.hk daily API)
- Legally registered and still active (record type: registry-active-global) [official record; status green] Indicates the company is not dissolved or winding down. checked 2026-09-06. Hong Kong Companies Registry, live local companies (data.cr.gov.hk daily API)
- On the company register (record type: registered-since) [official record; status green] On the company register since 1949-01-26. Shows how long the company has been on the state register, which is hard to fake and easy to check. checked 2026-09-06. Hong Kong Companies Registry, live local companies (data.cr.gov.hk daily API)
- Street address on file in the state register (record type: registered-address) [official record; status green] Registered address: 8/F DCH BLDG, 20 KAI CHEUNG RD, KOWLOON BAY, HONG KONG. The address the company itself gave the register, so post and inspectors reach it there. checked 2026-09-06. Hong Kong Companies Registry, live local companies (data.cr.gov.hk daily API)
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- HACCP
Import rules for these goods
- EU imports of food of animal origin and many other food categories must be pre-notified in TRACES and enter through border control posts. European Commission (TRACES)
- US imports require the foreign facility to be FDA-registered and the importer to run a Foreign Supplier Verification Program (FSVP). US FDA
- 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 whose products they sell and on what basis: a distribution agreement or the manufacturer's authorisation.