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CONSTELLATION® Vitrectomy Packs; CONSTELLATION® Phaco Packs; CONSTELLATION® Combined Procedure Packs; CONSTELLATION® Accessories (sipas listes bshkengjitur) - Albania Medical Device Registration

Access comprehensive regulatory information for CONSTELLATION® Vitrectomy Packs; CONSTELLATION® Phaco Packs; CONSTELLATION® Combined Procedure Packs; CONSTELLATION® Accessories (sipas listes bshkengjitur) in the Albania medical device market through Pure Global AI's free database. This Is;IIa;IIb medical device is manufactured by Alcon Laboratories, Inc. 6201 South Freeway, Forth Worth, Texas 76134-2099 USA. The device was registered on February 21, 2023.

This page provides complete registration details including product model (CONSTELLATION® Vitrectomy Packs; CONSTELLATION® Phaco Packs; CONSTELLATION® Combined Procedure Packs; CONSTELLATION® Accessories (sipas listes bshkengjitur)), manufacturer information, risk classification, and regulatory compliance data from the official Albania medical device database. Pure Global AI offers free access to Albania's medical device registry, helping global MedTech companies navigate Albania regulations efficiently.

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Albania Official Data
Is;IIa;IIb
CONSTELLATION® Vitrectomy Packs; CONSTELLATION® Phaco Packs; CONSTELLATION® Combined Procedure Packs; CONSTELLATION® Accessories (sipas listes bshkengjitur)
Albania Medical Device Registration
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Product Information

Pajisje mikrokirurgjikale qe perdoren se bashku ne aparatin Constellation vision, per procedura kirurgjikale te syrit.

Device Classification
Risk Class
Is;IIa;IIb
Product Model
CONSTELLATION® Vitrectomy Packs; CONSTELLATION® Phaco Packs; CONSTELLATION® Combined Procedure Packs; CONSTELLATION® Accessories (sipas listes bshkengjitur)
Product Name
CONSTELLATION® Vitrectomy Packs; CONSTELLATION® Phaco Packs; CONSTELLATION® Combined Procedure Packs; CONSTELLATION® Accessories (sipas listes bshkengjitur)
Registration Information
Registration Date
February 21, 2023
Analysis ID
13689.0