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Register / Egypt / DEA-EG-2022-0019
Egyptian Drug Authority · Egypt
DEA-EG-2022-0019
Tier 1 · Regulator-publishedUnclassifiedApreensão e destruiçãoStatus · active
Issuing authority
Egyptian Drug Authority (EDA)
Authority reference
Periodic report no.(19) For 2022
Date issued
27 Jul 2022
Recorded by us
2026-09-06 19:45:29 UTC
Produto
ICO SYRINGE STERILE HYPODERMIC SYRINGE 1ML
INN / active substance
Not stated by the issuing authority
Dosage form
Not stated by the issuing authority
Strength
Not stated by the issuing authority
Fabricante
Not stated by the issuing authority
Manufacturer country
Not stated by the issuing authority
MAH or importer
Not stated by the issuing authority
Números de lote
2205 · 2203
Prazos de validade
Not published with the notice
Action type
Apreensão e destruição
Classificação
Not stated by the issuing authority
Indicative severity
Not assessed by Drug Eye Africa
Defect category
Falsificado
Product type
Not stated by the issuing authority
ATC code
Not stated by the issuing authority
Affected markets
Egypt — no market beyond the issuing country was named on the notice
Cross-border event
Not linked to a cross-border event
Texto do aviso
@egyptiandrugauthority www.edaegypt.gov.eg 15301 ٧٢ يوليو ٢٢٠٢ تصنيع مصنع الدولية للمستلزمات الطبية وذلك )لكونهم غير مســـجلين وتم وضع رقم تسجيل خاص بمستلزم ٢٢اخـــر عليهم بالإضافـــة الى كونهم مخالفين للمنشـــور الدوري رقم الذي تم إصداره بناءً على قرار اللجنة المتخصصة بتسجيل ٦١٠٢ لســـنة المستلزمات الطبية( ضبط وتحريز كافة العبوات من المستلزمات الطبية الموضحة أدناه: منشور غش تجاري ICO SYRINGE STERILE HYPODERMIC SYRINGE 1ML تاريخ الانتهاء تاريخ الإنتاج اسم المستلزم رقم التسجيل 53/2011/15/2022 53/2011/1 ICO SYRINGE STERILE HYPODERMIC SYRINGE 1ML 3/2022 4/2027 2/2027 رقم التشغيلة 2205 2203
Original language: ar
Texto do aviso em inglês
Circular, July 2022. All packs of the medical devices described are to be impounded and seized, manufactured by the International Factory for Medical Supplies, on the grounds that they are unregistered, that a registration number belonging to a different device was placed on them, and that they contravene periodic circular number 22 of 2016 issued on the decision of the committee specialising in the registration of medical devices.
Machine translation, produced by Drug Eye Africa and not checked by the issuing authority. The authority stated only the text above it.
Estado
Em vigor
Superseded by
Not superseded. This is the current version.
Version
1

Provenance

Verification tier 1

Where this record came from, and what is held to show it.

Primary source
https://www.edaegypt.gov.eg/media/52zbnnnt/%D9%85%D9%86%D8%B4%D9%88%D8%B1-%D8%AF%D9%88%D8%B1%D9%8A-%D8%B1%D9%82%D9%85-19-%D9%84%D8%B3%D9%86%D8%A9-2022.pdf
Copy of the source
Taken and held by Drug Eye Africa, so the record survives the link above being moved or withdrawn. Not yet published at an address you can open.
Ask us for it and check it against the fingerprint below.
Fingerprint
00db16ac477042a42a967ce19a8f4d124f09a3cb315ed7e8f11d6d732fb6b8e1
SHA-256 of the copy held. Any file that produces this number is that copy, byte for byte; any file that does not is a different document.
Copy taken
2026-09-06 20:36:00 UTC

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DEA-EG-2026-0062Jun 2026EGCOLOVERIN-D 30 film Coated Tablets251035APublic warningUnclassifiedTier 1 · Regulator-published
DEA-EG-2026-0061Jun 2026EGFLOPADEX 8mg Hard gelatin capsules 302504626Public warningUnclassifiedTier 1 · Regulator-published
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Cite this record
Drug Eye Africa (2022). DEA-EG-2022-0019: ICO SYRINGE STERILE HYPODERMIC SYRINGE 1ML — Apreensão e destruição, Egyptian Drug Authority. Register of African Regulatory Actions. https://drugeyeafrica.org/register/notice/eg/2022/dea-eg-2022-0019

Version history

v1Manufacturer removed: the notice describes the packaging as counterfeit (correction)
—Corrections appear here and in the site-wide log. Records are superseded, never deleted.

Verification

Tier 1 — Published by the issuing regulator on its own channel and captured by Drug Eye Africa, with the source document archived.

Indexing

This record is indexable: it is dated, names a product, and carries either a batch number or a stated reason.

This record as data

/api/v1/notices/DEA-EG-2022-0019