VALENTINE INTERNATIONAL LTD.
詠立實業有限公司
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1Plants
9Certifications
< NT$20MRevenue band (est.)
- Unified Business No.
- 22428507
- Industry
- Plastic Products (7,565)
- Main products
- Plastic products (7,635)
- Location
- 8F, No. 147, 149, Sec. 2, Ta Tung Road, Hsichih Dist., New Taipei City 22183, Taiwan (R.O.C.)
New Taipei City (16,829) · Xizhi Dist. (1,300) - Listing
- Not publicly issued (84,625)
- Organisation type
- Limited Company
- Representative
- Chiu Yu-hsin
- Phone
- 02-86926662
- Exporter
- Yes — registered with the Trade Administration
- Annual revenue band
- < NT$20M estimated
- Ownership
- Individually held
- North American market
- FDA 510(k) clearance FDA medical device registration
- Representative tenure
- In office since at least 2024 (2+ years)
- Compliance record
- FDA import refusal: 1 product(s), latest 2020-09-14
Certifications 9
- Medical device license (Class I) (1,430)Official registry Valid until 2026-10-31 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2029-03-22 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2023-10-25 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2023-10-25 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2031-07-13 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2024-05-09 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2024-05-09 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2017-07-30 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2026-10-31 · Taiwan Food and Drug Administration (TFDA)
North American market evidence 4
- FDA 510(k) clearance K130017 2014-05-28
VALENTINE STEEL WHEELCHAIR - FDA 510(k) clearance K952196 1995-07-31
IV POLE/STAND - FDA medical device registration 8022890 1990-08-02 – 2026-06-15
Blood Pressure Cuff; Nebulizer (Direct Patient Interface); Device, Transfer, Patient, Manual and more (101) - FDA import refusal 3013742729 2020-09-14
CUSHION, FLOTATION
Recent changes 1
- Certification expiryMedical device license (Class I) certificate expired on 2026-10-31
RSS feed · Recent changes at Taiwanese manufacturers →
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