How to distinguish Class I or Class II medical devices directly from the product packaging?

Look at the registration number, the first digit of the XXXXXXXX number is the management category, 1 is a class 1, 2 is a class 2

The registration number is organized as follows:

× (×) 1 (food) Drug Supervision and Inspection of the mechanical (× 2) word ××××3 No. × 4 × × 5 ××××6. Where:

×1 for the registration and approval department of the location of the abbreviation:

International Class III medical devices, medical devices outside the country, as well as Taiwan, Hong Kong, Macao and medical devices for the "country";

International Class II medical devices for the registration and approval of the department is located in the province, autonomous region, Municipalities directly under the Central Abbreviations;

The first class of medical devices in the territory of the registration and approval department of the province, autonomous region, municipality directly under the Central Abbreviations plus the abbreviation of the municipal administrative region, as × × 1 (without the corresponding municipal administrative region, only for the province, autonomous region, municipality directly under the Central Abbreviations);

×2 for the form of registration (quasi, into the permit, permit):

The word "permit" applies to medical devices within the territory;

"In" applies to medical devices outside the territory;

"Permit" applies to medical devices in Taiwan, Hong Kong and Macao;

"Permit" applies to medical devices in Taiwan, Hong Kong, Macau;

××××3 is the year of approval for registration;

×4 is the product management category;

××5 is the product variety code;

××××6 is the registration number.