Medical Certifications
CE, CoA, Batch Reports, MOHAP — Every Document Explained
What each certification means, why UAE requires it, and exactly what Jazline provides on every medical shipment.
CE Certificate
Issued by: EU Notified Body
What It Is
Confirms the product meets EU safety, health and environmental requirements
Why UAE Needs It
UAE Ministry of Health (MOHAP) requires CE marking as a baseline for most medical device imports
What Jazline Provides
- CE certificate with notified body number
- Declaration of Conformity
- Technical file summary on request
Certificate of Analysis (CoA)
Issued by: Manufacturer / Third-Party Lab
What It Is
Documents the batch-specific physical, chemical and microbiological test results
Why UAE Needs It
MOHAP may request CoA at customs or for product registration. Batch numbers must match invoice.
What Jazline Provides
- CoA matching invoice batch numbers
- Third-party lab reports on request
- Sent before shipment leaves India
Batch Test Reports
Issued by: Accredited Laboratory
What It Is
Independent laboratory testing results for each production batch
Why UAE Needs It
Required for hospital and clinic procurement audits in UAE. DHA and HAAD suppliers often require these.
What Jazline Provides
- Batch test report for each order
- Accredited lab (NABL/ISO 17025)
- Sent proactively with shipment docs
MOHAP Import Permit
Issued by: UAE Ministry of Health
What It Is
UAE Ministry of Health and Prevention permit required for most medical device imports
Why UAE Needs It
Without MOHAP permit, shipment may be held at UAE customs indefinitely
What Jazline Provides
- MOHAP guidance note per HS code
- Product registration advisory
- Importer permit application support
Need the Full Document Pack?
Send your HS code and quantity. We send the full cert pack within 4 hours.
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