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"Akrus" Non-AC-powered patient lift (Non-Sterile) - Taiwan Registration 2e1e6c8a0f2f32dcda246e17df28a3a9

Access comprehensive regulatory information for "Akrus" Non-AC-powered patient lift (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2e1e6c8a0f2f32dcda246e17df28a3a9 and manufactured by AKRUS GMBH & CO. KG. The authorized representative in Taiwan is NAN KAI CORPORATION.

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2e1e6c8a0f2f32dcda246e17df28a3a9
Registration Details
Taiwan FDA Registration: 2e1e6c8a0f2f32dcda246e17df28a3a9
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Device Details

"Akrus" Non-AC-powered patient lift (Non-Sterile)
TW: "่‰พๅกๆ–ฏ"้žไบคๆต้›ปๅŠ›ๅผ็—…ๆ‚ฃๅ‡้™ๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2e1e6c8a0f2f32dcda246e17df28a3a9

Ministry of Health Medical Device Import No. 015285

DHA09401528507

Company Information

Germany

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".

J General hospital and personal use equipment

J5510 Non-AC Electric Patient Lift

Imported from abroad

Dates and Status

Jun 02, 2015

Jun 02, 2025