Hutzel Dreh Tech GmbH

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.

HutzelTechnics グループの精密部門は、世界中のさまざまな材料で作られた精密部品のための革新的なソリューションを実装しています。精密部品、自動化システム、医療技術向けの革新的なソリューション。 HutzelTechnics グループは、精密、オートメーション、医療機器の各部門を擁し、ドイツ製の絶対的な信頼性、チームワーク、業界を超えた専門知識を象徴しています。完璧に調整された生産プロセス、最先端の機械、革新的なテクノロジーにより、成功と継続的な開発が保証されます。コンサルティングからデベロッパーまで、幅広いポートフォリオを提供しています。

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: Steinenbronn, Germany
Founded: 1948 (from our catalogue record; not confirmed by the company or by a state register)
Website: hutzeltechnics.de
Categories: 医療およびヘルスケア用品, 産業機械

Listed in a source registry

Europages B2B directory

What is established and what is not

No researcher review has been written for this company yet. 2 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

First recorded on the web archive (record type: web-presence-since) [our own observation, not an official record; status green] The web archive holds a page at this address from 2014. Shows a web archive saw a page at this address on that date. It does not show who ran the site then. checked 2026-08-07. Internet Archive (Wayback)
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 2026-08-16. 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 2026-08-16. OpenSanctions
manufacturing-practice-certified (record type: manufacturing-practice-certified; this record does not by itself establish manufacturing) [official record; status green] A regulator of health products inspected this site and certified how it manufactures the product class named, for example medical devices or cosmetics. It is about manufacturing practice at the site, not a medicines licence. checked 2026-10-17. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-08-01. VIES (European Commission)

Relationships

4 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.

Recorded in a source

GEWERBESTR. 5, 71144 STEINENBRONN, ALEMANHA: Manufactures at the site. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)

Candidates, not confirmed

Czechia: Site named by the company itself, not confirmed by a record, country CZ. hutzeltechnics.de
Germany: Site named by the company itself, not confirmed by a record, country DE. hutzeltechnics.de
hutzeltechnics.de: Website of this business. Source record

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)
Machinery sold in the EU needs CE marking with a declaration of conformity under the EU machinery rules. European Commission
No public registry exists for certificates of this kind in this sector: conformity is declared by the manufacturer. European Commission: CE marking, manufacturer's conformity assessment

Check independently

Before a first order, ask for the production site address and a document linking that site to this legal entity.

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