GETEX LENZ Technische Textilien GmbH
50 多年来，我们专注于剪裁、鳍片 Getex Lenz - 您的产业用纺织品、魔术贴和紧固系统的合作伙伴 50 多年来，我们专注于技术纺织品以及紧固系统的裁剪、整理和加工，适用于从医疗技术到工业应用等各个行业。 我们的优势： ✔ 定制解决方案 -
50 多年来，我们专注于剪裁、鳍片 Getex Lenz - 您的产业用纺织品、魔术贴和紧固系统的合作伙伴 50 多年来，我们专注于技术纺织品以及紧固系统的裁剪、整理和加工，适用于从医疗技术到工业应用等各个行业。 我们的优势： ✔ 定制解决方案 - 根据客户规格进行个性化制造 ✔ 最高品质 - 精确的加工和可靠的交货时间 ✔ 灵活性 - 小批量、定制设计、样品创建和快速响应时间 ✔ 创新产品开发 - 从原型开始
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Göppingen, Germany
- Founded
- 1972
- Website
- getex-lenz.de
- Categories
- 医疗保健用品, 面料及纺织材料
- Markets
- 德国
Listed in a source registry
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