GETEX LENZ Technische Textilien GmbH

Listed in a source registry

Europages B2B directory

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

• vat-valid (green), checked 2026-08-13 VIES (European Commission)
• sanctions-clear (green), checked 2026-08-15 OpenSanctions
• debarment-clear (green), checked 2026-08-15 OpenSanctions
• energy-market-role (green), effective since 2019-09-05 Marktstammdatenregister (Bundesnetzagentur)

Claimed certifications, not confirmed by us

• ISO 9001, Quality Management IAF CertSearch

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)
• Textiles sold in the EU must carry fibre-composition labelling under Regulation (EU) No 1007/2011. European Commission
• Textiles sold in the US must comply with FTC labeling rules (fiber content, country of origin, care instructions). US FTC

Check independently

• Sanctions and watchlists (OpenSanctions)
• VAT number check (EU VIES)