Identity
- Trade Name
- EX-PRESS® FDA UDI
- Generic Name
- Glaucoma shunt FDA UDI
- Device Name
- EX-PRESS® Glaucoma Filtration Device - Version P-200 FDA UDI
- Model / Reference
- P-200 FDA UDI
- Description
- EX-PRESS® Glaucoma Filtration Device - Version P-200 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00380650704948 FDA UDI
- FDA Product Code
- KYF FDA UDI
- GMDN Term
- Glaucoma shunt FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.3920 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 200 Micrometer FDA UDI
Ex-Press® by Alcon Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Alcon Laboratories, Inc.
Sources (1)
- FDA UDI 7239a1de-6042-4a14-bd5e-aa69763840c7 36 fields · synced Jun 8, 2026