Gold Member Since 2004
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Shanghai Pharmaceutical Machinery Co., Ltd.

Pill Making Equipment, Press Equipment, Pressing Machine manufacturer / supplier in China, offering Gzpl-680 Double Sided High-Speed Rotary Pill Making Equipment, Gzl6 Vacuum Freeze Dryer for Pharmaceuticals, High Quality Dxd-80 Microcomputer Packaging Machine and so on.

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Supplier Homepage Product Tablet Press Machine Gzpl-680 Double Sided High-Speed Rotary Pill Making Equipment

Gzpl-680 Double Sided High-Speed Rotary Pill Making Equipment

FOB Price: US $293,000 / Set
Min. Order: 1 Set
Min. Order FOB Price
1 Set US $293,000/ Set
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Production Capacity: 758000tablets/H
Transport Package: Standard Export Wooden Cases
Payment Terms: L/C, T/T, D/P, Western Union, Paypal, Money Gram

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Basic Info
  • Model NO.: GZPL-680
  • Finished Dosage Form: Tablet
  • Certification: CE, GMP, ISO, SGS
  • Computerized: Computerized
  • Condition: New
  • Weight: 4800kg
  • Noise: Less Than 85 Dba
  • Max. Tablet Thickness: 8.5mm
  • Specification: GMP and FDA.
  • HS Code: 8479820090
  • Type: Preparation Machinery
  • Precision: High Precision
  • Voltage: 380V
  • Customized: Customized
  • Warranty: 1 Year
  • Rated Power: 14kw
  • Max.Mian Compression Force: 100kn
  • Trademark: SPM
  • Origin: China
Product Description

Basic Info.
Model NO.:GZPL-680
 
Type:Preparation Machinery
Finished Dosage Form:Tablet
 
Precision:High Precision
Certification:CE, GMP, ISO, SGS
 
Voltage:380V
Computerized:Computerized
 
Customized:Customized
Condition:New
 
Warranty:1 Year
Export Markets:Global
Product Description
GZPL-680 Series High Speed Tablet Press is developed independently and newly produced by 
SPM. With advanced design and control technology, it is in a leading position domestically; Making 
advantage of own intellectual property, the main performances reach the international level in 
compliance with requirement of GMP and FDA.


Features:  
Design of GMP & FDA
Same main and precompression
Interchangeable turret
Control by servo motor
 
Electronic record and signature in compliance with FDA 21 CFR Part 11

 
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