Mandatory Implementation date Ç¿ÖÆʵʩÈÕÆÚ
A transition period is provided in the rules allowing use of the former DoC or verification procedures, whichever was previously applicable for a device, until November 2, 2018.
2017Äê11ÔÂ2ÈÕ£¬ÃÀ¹úÁª°îͨÐÅίԱ»á£¨FCC£©³ǫ̈Îļþ£¬½«FCC DoC & Verification ÈÏÖ¤³ÌÐòºÏ²¢³ÉSDoC£¬¹ý¶ÉÆÚΪһÄ꣬¼´2018Äê11ÔÂ2ÈÕÆðFCC ½«Ê¹ÓÃSDoC ÈÏÖ¤³ÌÐò¡£
SDoCÈÏÖ¤ÒªÇó
SDoCÊDzúÆ·ÔðÈη½È·±£²úÆ·ÇкÏÆäÏà¶ÔÓ¦¼¼Êõ±ê×¼ÒªÇóµÄ³ÌÐò
¨CThe responsible party, who must be located in the United States (provide their name, address and telephone number or internet contact information)²úÆ·ÔðÈη½±ØÐëÔÚÃÀ¹ú±¾ÍÁ, ÇÒ±ØÐëÒªÓÐÔðÈη½µÄÁªÏµÐÅÏ¢.
¨Cis not required to file an equipment authorization application with the Commission or a TCB.
SDoCÈÏÖ¤²»ÐèҪͨ¹ýFCCίԱ»á»òTCBÉóºËÅú×¼.
¨CEquipment authorized under the SDoC procedure is not listed in a Commission database.
SDoCÈÏÖ¤µÄ²úÆ·×ÊÁϲ»»áÉÏ´«ÖÁFCC¹Ù·½µÄÊý¾Ý¿â.
¨CThe responsible party or any other party marketing the equipment must provide a test report and other information demonstrating compliance with the rules upon request by the Commission.
²úÆ·ÔðÈη½»òÆäËüÍÅÌå±ØÐëÌṩ¼ì²â±¨¸æºÍίԱ»áÒªÇóÖ¤Ã÷ÆäÇкϹæÔòµÄ×ÊÁÏ.
¨CThe responsible party has the option to use the certification procedure in place of the SDoC procedure.
²úÆ·ÔðÈη½¿ÉÒÔÑ¡ÔñʹÓÃCertification ÈÏ֤ȡ´úSDoCÈÏÖ¤.
¨CEquipment approved using SDoC is required to be tested, however, it is not necessary to use an FCC-recognized accredited testing laboratory. SDoCÈÏÖ¤²¢·×Æ綨ҪÔÚFCC¹«ÈϵÄʵÑéÊÒÀï½øÐвâÊÔ.
Product¡¯s Labeling ²úÆ·±êÇ©
¨CDevices subject to SDoC are required to be uniquely identified by the responsible party prior to importing the equipment to or marketing it in the United States.
SDoCÈÏÖ¤µÄ²úÆ·ÔÚÏòÃÀ¹ú½ø¿Ú»òÏúÊÛÇ°, ±ØÐëÒªÓÐÔðÈη½µÄΨһ±êʶ
¨CDevices subject to authorization under SDoC can be labeled with the following FCC logo on a voluntary basis.
SDoCÈÏÖ¤µÄ²úÆ·, LabelÊÇ·ñҪʹÓÃFCC LogoÊÇ×ÔÔ¸µÄ.
Applicable Product ÊÊÓõIJúÆ·
FCC Part15B-unintentional radiatorsÕë¶ÔÊÊÓÃÓÚFCC Part15µÄ·ÇÒâͼ·øÉä²úÆ·£¬ÈÏÖ¤·½·¨ÐÞ¸ÄÈçÏ£º
PART 18¡ªIndustrial, Scientific, and Medical EquipmentÕë¶ÔÊÊÓÃÓÚFCC Part18µÄÒâͼ·øÉä²úÆ·£¬ÈÏÖ¤·½·¨ÐÞ¸ÄÈçÏÂ:
Consumer ISM equipment, unless otherwise specified, must be authorized under either the Supplier's Declaration of Conformity or the certification procedure prior to use or marketing
Ïû·ÑÀ๤¿ÆÒ½É豸±ØÐëÑ¡ÔñSDoC»òCertificationÈÏ֤ȥÏúÊÛ.
Compliance Information ÇкÏÐÅÏ¢
¨C²úÆ·ÐÅÏ¢Identification of the product, e.g., Trade name and model number;
¨C²úÆ·ÔðÈη½µÄÐÅÏ¢The identification, by name, address, and telephone number, or internet contact information, of the responsible party. The responsible party must be located within the United States
¨CÇкϹæÔòµÄÐÅÏ¢A statement that the product complies with the rules, e.g., FCC part15.19(a)(3)
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