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此帖為韓國 KFDA 申請流程和提供的資料
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% K J/ g @7 S9 f, |; l0 G: i1. General Information & _6 J3 k% u+ q: Z
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1) Manufacture Certificate (Free Sales Certificate) and ISO13485 : in case of USA, CFG.
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2) Manuals: Op manual, SVC Manual, Pre-installation Manual etc. # k8 G9 L" _& M
" W1 ^: W! D& b$ W7 g3) IEC Test Report : 60601-1, 60601-2 etc.
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4) Performance Test Report, Final Test Report etc. .
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' z5 D2 ~/ t& u, c3 K x( w0 A5) Data sheet
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6) Catalog / Q" s/ _, h' O: h/ v$ e V
* h- \! ?# y' Q; R _7) Part List 1 B; T5 s* h! e+ |9 A9 {) P
9 x' y% r9 `, P1 t8) Software Validation Report ' R% L i7 v0 S
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2. below contents should be commented 6 |8 s$ R& a" t5 R$ u2 f
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A. Raw materials, Specification of each components (ISO, IEC ASTM etc), Model name of each components
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B. External appearance photos, internal structure, sizes, weight
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% r3 s2 w) k8 F1 a, {C. Block diagram of system, Circuit diagram of power supply, Protection degree of electrical shock;
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D. Manufacturing methods or flow chart; % @' Y: W2 A( w3 Z' P
/ f8 e2 j% M+ VE. Specification of the system 9 q8 F5 a& O) _
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F. Effectiveness, purpose of use, intended use; $ \) q' v: |0 W8 j k
+ j& T: ^& e$ RG. Instructions for use;
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H. Precautions in use; ! ^1 ?& R9 @& C0 t. c9 M& N
3 o; I& X! [# m9 P5 AI. Storage methods;
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J. Information on origin, discovery and background of development (reference, articles)
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K. Information on determination of structure and physicochemical and biological properties (in case of concerned)
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L. Stability data - Toxicity data (for only human contact material) 7 ?7 S- b/ k. l( D. U8 Y& K
8 u* L9 g" S0 V+ F1 `4 B8 gM. Sterilization method, condition, Deterioration test etc(in case of concerned) 0 C6 B6 |6 P# u% u
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N. Clinical study report Foreign clinical studies may be accepted in lieu of local trials. KFDA requires that such studies be conducted according to Good Clinical Practices (GCP). KFDA's preference is a final report of a clinical study published by a reputable professional journal listed on the Science Citation Index. However, KFDA will review unpublished study reports to determine acceptability, depending on GCP compliance and the reputation of the research organization involved. |
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