New regulations for import and export of dairy products will be implemented in May

New regulations for import and export of dairy products will be implemented in May The new version of the "Administrative Measures on Inspection and Quarantine of Imported and Exported Dairy Products" will be implemented starting May 1. Recently, the AQSIQ issued an announcement on the new measures.

The new version of the "Measures" pointed out that the range of dairy products to which the "Measures" are applied should be adjusted and published on the website of the AQSIQ. The milk powder prescribed in Article 2 of the Measures includes bovine colostrum powder; milk-based infant formula foods include base powder raw materials. The "means" are not applicable to infant formulas for special medical purposes. For the first time imported dairy products, importers or their agents, they should provide inspection reports for the items listed in the national standards for food safety of the corresponding products, including the standards for contaminants and mycotoxins in foods cited in the standard. For dairy products that are not imported for the first time, the importer or its agent should provide the inspection report and the copy of the inspection report provided at the time of the first import, as well as the test report of the project stipulated by the General Administration of Quality Supervision, Inspection and Quarantine. Non-first-time import inspection report items are adjusted and determined by the State General Administration of Quality Supervision, Inspection and Quarantine (AQSIQ) on the basis of the monitoring of dairy product risk, and published on the website of the General Administration of Quality Supervision, Inspection and Quarantine. For the first time imported infant formula food powder raw materials (milk-based premixes), importers or their agents, they should provide inspection reports on microorganisms, pollutants, and mycotoxin items as specified in the product standards. Non-primary imported ground powder raw materials should provide inspection reports for microbiological projects.

The new version of the "Regulations" emphasizes that when imported dairy safety and health items are not qualified, the importer or its agent shall continue to provide 5 batches (referring to 5 different production batches or production dates) to provide the corresponding national standards for food safety. The test report of the project (including the pollutants and mycotoxins cited in the standard). If the unqualified item is detected as an illegal additive, the test report shall include the item. Importers of imported dairy products should timely disclose the types, origins, brands, etc. of imported dairy products through public-facing media (including the official website of the company). In addition, importers of imported dairy products should timely disclose the types, origins, brands, etc. of imported dairy products through public-facing media (including the official website of the company). For unqualified imported dairy products that need to be destroyed or returned for processing, after the importer completes the destruction or returns, it should report the destruction or return to the inspection and quarantine authorities within 5 working days.

Patient Monitor

Features
10.1 inch high resolution color TFT display
Lightweight and portable design suitable for Ambulance,Emergency Transport
Three Working Modes : Monitoring , Surgery and Diagnosis.
Simple and friendly operating display interface.
Multi-display modes suitable for different applications: Standard Interface , Large font , ECG Standard Full Display ,OXY, Trend able BP Trend.
Built-in high capacity battery up to 3 hours of continuous work


Technique Specification
ECG

Lead Mode : 5 Leads ( I , ll , Ill , AVR , AVL , AVF , V )
Gain : 2.5mm / mV, 5.0mm /mV , 10mm /Mv, 20mm /mV
Heart Rate : 15-300 BPM ( Adult ) ; 15-350 BPM ( Neonatal )
Resolution : 1 BPM
Accuracy : ± 1%
Sensitivity > 200 uV ( Peak to peak )
ST measurement range : -2.0 ~+ 2.0 Mv
Accuracy : -0. 8mV~+ 0. 8mV : ± 0. 02mV or ± 10% , which is greater
Other Range : unspecified
Sweep speed : 12.5 mm / s , 25mm / s , 50mm / s
Bandwidth:
Diagnostic : 0.05~130 Hz
Monitor : 0.5~40 Hz
Surgery : 1~20 Hz

SPO2
Measuring Range : 0 ~ 100%
Resolution : 1%
Accuracy : 70%~100% ( ± 2 % )
Pulse Rate : 20-250 BPM
Resolution : 1 BPM
Accuracy : ± 3 BPM

Optinal Parameters :
Central monitoring system
Dual IBP
Etco 2
12-lead ECG
Nellcor SpO2
Sun Tech NIBP

NIBP
Method : Oscillometry
Measure mode Manual, Auto, STAT
Unit : mmHg , kPa
Measure and alarm range:
Adult Mode
SYS 40 ~ 280 mmHg
DIA 10 ~ 225 mmHg
MEAN 20 ~ 240 mmHg

Pediatric Mode
SYS 40 ~ 220 mmHg
DIA 10 ~ 160 mmHg
MEAN 20 ~ 170 mmHg

Neonatal Mode
SYS 40 ~ 135 mmHg
DIA 10 ~ 100 mmHg
MEAN 20 ~ 110 mmHg
Resolution : 1 mmHg
Accuracy : ± 5 mmHg

TEMP
Measure and Alarm Range : 0 ~ 50 C
Resolution : 0 . 1C
Accuracy : ± 0 . 1C

Standard Parameters
ECG, RESP, TEMP, NIBP, SPO2, PR

RESP
Method : Impedance between RA-LL or RALA
Measurement Range:
Adult : 10~120 BrPM
Neonatal / Pediatric : 7~150 BrPM
Resolution : 1 BrPM
Accuracy : ± 2 BrPM

Standard Configuration
No Item Qty

  1. 1 Main Unit 1
  2. 2 5-lead ECG cable 1
  3. 3 Disposable ECG Electrode 5
  4. 4 Adult Spo2 probe 1
  5. 5 Adult NIBP cuff 1
  6. 6 NIBP extension tube 1
  7. 7 Temperature probe 1
  8. 8 Power Cable 1
  9. 9 User Manual 1
  10. 10 Fuse 3

Patient Monitor,Portable Patlent Monltor,Patlent Monltor For Adult,Patlent Monltor For Baby

Guangzhou Sonostar Technologies Co., Limited , https://www.sonoeye.com

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