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.
进口全球医疗产品和食品的主要分销引擎
我们管理冷链肉类、临床药品、医疗保健电子产品的大规模进口。我们的网络向医院、酒店和主要零售店提供服务。
- 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
- 冷冻和冷藏食品, 特色美食, 医疗保健用品
- Markets
- 中国香港特别行政区, 中国澳门特别行政区
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.