Identity
- Trade Name
- Ahmed ClearPath ST FDA UDI
- Generic Name
- Glaucoma shunt, tubular, non-animal-derived FDA UDI
- Device Name
- Glaucoma shunt FDA UDI
- Model / Reference
- ST350 FDA UDI
- Description
- Glaucoma shunt FDA UDI
Identifiers
- Catalog Number
- 10-0610 FDA UDI
- Primary DI / UDI-DI
- 00892064002096 FDA UDI
- FDA Product Code
- KYF FDA UDI
- GMDN Term
- Glaucoma shunt, tubular, non-animal-derived FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.3920 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
MR Safe FDA UDI
Dimensions & Sizes
- Size
- Area/Surface Area — 350 Square millimeter FDA UDI
Category: Glaucoma shunt, tubular, non-animal-derived
Ahmed ClearPath ST by New World Medical, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Glaucoma shunt, tubular, non-animal-derived.
- Ahmed ClearPath ST — NEW WORLD MEDICAL, INCORPORATED · Class II
- Ahmed™ Glaucoma Valve — NEW WORLD MEDICAL, INCORPORATED · Class II
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
- New World Medical, Incorporated
Sources (1)
- FDA UDI 6d81bc06-c27e-46fd-802c-75eb40c1c32c 36 fields · synced Jun 8, 2026