FDA UDI In Commercial Distribution 🇺🇸 United States

EX-PRESS

DI: 00380650500045 · Model: P-50 · Alcon Laboratories, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
EX-PRESS
Primary DI
00380650500045
Version / Model
P-50
Catalog Number
8065050004
Company Name
Alcon Laboratories, Inc.
Labeler DUNS
008018525
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-23
Public Version
1
Public Version Date
2025-10-01
Public Version Status
New
Public Device Record Key
12cc3b3c-ac0c-4132-9e86-d5e06b7a741e

Device Description

EX-PRESS Glaucoma Filtration Device - Version P-50

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KYF Implant, Eye Valve

GMDN Terms

Code Name
42526 Eye valve

Identifiers

Type ID
Primary 00380650500045

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 50 Micrometer