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Ahmed™ Glaucoma Valve

FDA UDI

Class II (US FDA UDI)

by New World Medical, Incorporated

Identity

Trade Name
Ahmed™ Glaucoma Valve FDA UDI
Generic Name
Eye valve FDA UDI
Device Name
Polypropylene Glaucoma Drainage Device FDA UDI
Model / Reference
S2 FDA UDI
Description
Polypropylene Glaucoma Drainage Device FDA UDI

Identifiers

Catalog Number
S2 FDA UDI
Primary DI / UDI-DI
00892064002133 FDA UDI
510(k) Number
K925636 FDA UDI
FDA Product Code
KYF FDA UDI
GMDN Term
Eye valve 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

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
Sterilization Method
Radiation Sterilization FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Area/Surface Area — 184 Square millimeter FDA UDI

Ahmed™ Glaucoma Valve by New World Medical, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
New World Medical, Incorporated

Sources (1)

  • FDA UDI 86ac5462-cff0-45be-a2b7-0d1d4153daac 38 fields · synced May 30, 2026