Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2022
50000 ㎡
200
Machinery Directive Attestation of Conformity for ZFG Series Pulp Molding Equipment, Machinery Directive Attestation of Conformity for Pulp Molding Equipment
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)
Since 2013
51,985 m²
235
FDA Establishment Registration & Device Listing, 510 (k) Premarket Notification, Quality Management System Certificate, EU Quality Assurance Certificate (MDR), EU Quality Management System Certificate (MDR)