Ce Full Quality Assurance Certificate : Ce Certificate Of X Ray Machine Perlong Medical Equipment Co Ltd : Directive 93/42/eec on medical devices, annex ii excluding section 4.

Supplementary information to ce 01085. Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 565719. The ce mark is only intended to be used on. Directive 93/42/eec on medical devices (mdd), annex il excluding (4).

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(devices in class lla, ilb or iii). Directive 93/42/eec on medical devices (mdd), annex il excluding (4). Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 01085. Supplementary information to ce 683722. Directive 93/42/eec on medical devices, annex ii excluding section 4. The ce mark is only intended to be used on. Directive 93/42/eec on medical devices, annex ii excluding section 4.

(devices in class lla, ilb or iii).

(devices in class lla, ilb or iii). Must affix the ce marking to each item of pressure equipment and draw up a written declaration of conformity. Supplementary information to ce 683722. Directive 93/42/eec on medical devices, annex ii excluding section 4. Directive 93/42/eec on medical devices, annex ii excluding section 4. Directive 93/42/eec on medical devices (mdd), annex il excluding (4). Supplementary information to ce 01085. Supplementary information to ce 565719. Supplementary information to ce 641036. Directive 93/42/eec on medical devices, annex ii excluding section 4. Full quality assurance / module h : Supplementary information to ce 688840. The ce mark is only intended to be used on.

Supplementary information to ce 688840. Supplementary information to ce 01085. Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 565719. Directive 93/42/eec on medical devices (mdd), annex il excluding (4).

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Supplementary information to ce 01085. (devices in class lla, ilb or iii). Must affix the ce marking to each item of pressure equipment and draw up a written declaration of conformity. Full quality assurance / module h : Directive 93/42/eec on medical devices (mdd), annex il excluding (4). Directive 93/42/eec on medical devices, annex ii excluding section 4. The ce mark is only intended to be used on. Supplementary information to ce 565719.

Directive 93/42/eec on medical devices, annex ii excluding section 4.

Directive 93/42/eec on medical devices (mdd), annex il excluding (4). (devices in class lla, ilb or iii). Supplementary information to ce 683722. Supplementary information to ce 641036. Supplementary information to ce 688840. Full quality assurance / module h : Directive 93/42/eec on medical devices, annex ii excluding section 4. Directive 93/42/eec on medical devices, annex ii excluding section 4. Must affix the ce marking to each item of pressure equipment and draw up a written declaration of conformity. Directive 93/42/eec on medical devices, annex ii excluding section 4. The ce mark is only intended to be used on. Supplementary information to ce 01085. Supplementary information to ce 565719.

Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 01085. Full quality assurance / module h : Must affix the ce marking to each item of pressure equipment and draw up a written declaration of conformity. The ce mark is only intended to be used on.

Directive 93/42/eec on medical devices, annex ii excluding section 4. Bio Science Org — Bio Science Org from

Full quality assurance / module h : Directive 93/42/eec on medical devices, annex ii excluding section 4. Must affix the ce marking to each item of pressure equipment and draw up a written declaration of conformity. Directive 93/42/eec on medical devices (mdd), annex il excluding (4). (devices in class lla, ilb or iii). Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 688840. The ce mark is only intended to be used on.

Supplementary information to ce 565719.

Supplementary information to ce 641036. Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 565719. Full quality assurance / module h : Directive 93/42/eec on medical devices (mdd), annex il excluding (4). Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 01085. (devices in class lla, ilb or iii). Supplementary information to ce 683722. The ce mark is only intended to be used on. Supplementary information to ce 688840. Directive 93/42/eec on medical devices, annex ii excluding section 4. Must affix the ce marking to each item of pressure equipment and draw up a written declaration of conformity.

Ce Full Quality Assurance Certificate : Ce Certificate Of X Ray Machine Perlong Medical Equipment Co Ltd : Directive 93/42/eec on medical devices, annex ii excluding section 4.. Directive 93/42/eec on medical devices, annex ii excluding section 4. Directive 93/42/eec on medical devices (mdd), annex il excluding (4). Directive 93/42/eec on medical devices, annex ii excluding section 4. Supplementary information to ce 688840. Directive 93/42/eec on medical devices, annex ii excluding section 4.