CAREMED SUPPLY INC.
繁葵實業股份有限公司
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1997Founded
NT$272MPaid-in capital
3Plants
21Certifications
11Patents
NT$20–100MRevenue band (est.)
- Unified Business No.
- 97404268
- Industry
- Other Manufacturing (2,432)
- Main products
- Medical devices & supplies (878)
- Location
- 7F., NO.2, LANE 235, BAO CHIAO RD., XINDIAN DIST., NEW TAIPEI CITY 231028, TAIWAN (R.O.C.)
Yilan County (1,016) · Wujie Township (243) - Listing
- Not publicly issued (84,625)
- Registration status
- Approved / Active
- Organisation type
- Company Limited by Shares
- Founded
- 1997-03-21
- Paid-in capital
- NT$ 271,979,030
- Representative
- Liu Tsung-hsuan
- Phone
- 02-29179808
- Website
- https://caremed.com.tw
- Exporter
- Yes — registered with the Trade Administration
- Annual revenue band
- NT$20–100M estimated
- Ownership
- Individually held
- North American market
- FDA 510(k) clearance FDA medical device registration Health Canada medical device licence
- Representative tenure
- In office since 2019-09 (7 yrs); last handover 2019-09 (same surname)
- Compliance record
- FDA import refusal: 1 product(s), latest 2025-12-18
Plants 3
- Yilan Sanjie Plant · 2F, No. 50, Ln. 30, Sanjie 2nd Rd., Wujie Township, Yilan County In production
- Yilan Xin Plant 5 · No. 18, 20, Xinwu Rd., Wujie Township, Yilan County In production
- Plant · 6, 7F, No. 2, Ln. 235, Baoqiao Rd., Xindian Dist., New Taipei City In production
Certifications 21
- Medical device license (Class I) (1,430)Official registry Valid until 2028-09-26 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2025-08-14 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2030-12-03 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2014-08-20 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2024-10-31 · 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)
- Medical device license (Class I) (1,430)Official registry Valid until 2015-11-29 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2011-12-08 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2010-10-28 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2015-10-04 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2015-11-17 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2015-11-19 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2011-03-29 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2015-09-24 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2010-10-30 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2010-10-30 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2011-11-23 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class I) (1,430)Official registry Valid until 2027-10-31 · Taiwan Food and Drug Administration (TFDA)
- Medical device license (Class II) (794)Official registry Valid until 2031-05-09 · Taiwan Food and Drug Administration (TFDA)
- GMP (261)Self-reported
- ISO 13485 (310)Self-reported
Patents 11
- 2025 Foldable mattress
- 2024 Inflatable mattress
- 2024 Mattress with replaceable layer body and packaging material
North American market evidence 6
- FDA 510(k) clearance K181217 2018-08-05
VesoFlow Lite DVT Compression Device - FDA 510(k) clearance K141064 2014-12-04
VESOFLOW PLUS DVT COMPRESSION DEVICE - FDA medical device registration 8022590 2009-09-22 – 2023-12-11
Sleeve, Limb, Compressible; Mattress, Flotation Therapy, Non-Powered; Bed, Ac-Powered Adjustable Hospital and more (6) - FDA medical device registration 3013528589 2011-09-14 – 2021-04-29
Sleeve, Limb, Compressible; Mattress, Air Flotation, Alternating Pressure; Device, Transfer, Patient, Manual and more (4) - FDA import refusal 3013528589 2025-12-18
SLEEVE, LIMB, COMPRESSIBLE - Health Canada medical device licence 119437
Recent changes 1
- Certification expiryMedical device license (Class I) certificate expired on 2026-10-31
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