UFP Technologies, Inc.
Medikal ve endüstriyel sektörlere yönelik özel köpük, elyaf ve ambalaj çözümleri.
UFP Technologies, yenilikçi özel ambalajlar, bileşenler ve köpük, elyaf ve özel dönüştürücü malzemelerden yapılmış ürünlerin tasarımcısı ve üreticisidir. Tıbbi segmenti, cihaz üreticileri için köpük bazlı cerrahi konumlandırma sistemleri, özel tıbbi ambalajlar ve temiz oda uyumlu bileşenler üretmektedir. Şirket ayrıca endüstriyel, havacılık ve tüketici ürünleri koruma uygulamaları için özel poliüretan köpük ve kalıp kesim ambalajlar da tedarik ediyor.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Newburyport, MA, United States
- Founded
- 1963
- Website
- ufpt.com
- Categories
- Ambalaj ve Baskı Malzemeleri, Tıbbi ve Sağlık Malzemeleri, Endüstriyel Malzemeler
- Markets
- Amerika Birleşik Devletleri, Kanada, Almanya, Birleşik Krallık
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
- corporate-mail-on-domain (green), checked 2026-08-10 Mail server of the company domain
- debarment-clear (green), checked 2026-08-10 OpenSanctions
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- domain-registered (green), checked 2026-08-10 Domain registry record
- fda-registered (green), checked 2026-08-10 FDA
- fda-contract-manufacturer (green), checked 2026-08-10 FDA
- sanctions-clear (green), checked 2026-08-10 OpenSanctions
- registry-id-verified (green), checked 2026-09-10 GLEIF Global LEI record
Claimed certifications, not confirmed by us
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality 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)
- If the goods are paper, board or printed products, EU imports fall under the Deforestation Regulation (EUDR) due-diligence regime; packaging machinery itself does not. European Commission (EUDR)