7 Meddev Solutions Limited (RAPS e-Book version)
Contents
Article 93: Market surveillance activities 234
Article 94: Devices with unacceptable risk or noncompliance 235
Article 95: Dealing with devices presenting unacceptable risk 236
Article 96: Evaluating national measures at Union level 237
Article 97: Other non-compliance 238
Article 98: Preventive health protection measures 239
Article 99: Good administrative practice 240
Article 100: Electronic system on market surveillance 241
Article 101: Competent authorities 242
Article 102: Cooperation 244
Article 103: Medical Device Coordination Group 245
Article 104: Support by the Commission 246
Article 105: Tasks of the MDCG 247
Article 106: Provision of opinions and advice 249
Article 107: Conflict of interests 250
Article 108: Device registers and databanks 251
Article 109: Confidentiality 252
Article 110: Data protection 254
Article 111: Levying of fees 255
Article 112: Funding of activities related to notified bodies 256
Article 113: Penalties 257
Article 114: Committee procedure 258
Article 115: Exercise of the delegation 259
Article 116: Separate delegated acts for delegated powers 260
Article 117: Amendment to Directive 2001/83/EC 261
Article 118: Amendment to Regulation (EC) No 178/2002 262
Article 119: Amendment to Regulation (EC) No 1223/2009 263
Article 120: Transitional provisions 264
Article 121: Evaluation 265
Article 122: Repeal 266
Article 123: Entry into force and date of application 267