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Susvimo

FDA UDI

Class N (US FDA UDI)

by Genentech, Inc.

Identity

Trade Name
SUSVIMO FDA UDI
Generic Name
Implantable intraocular medication reservoir FDA UDI
Device Name
SUSVIMO INSERTION TOOL ASSEMBLY FDA UDI
Model / Reference
4000120 FDA UDI
Description
SUSVIMO INSERTION TOOL ASSEMBLY FDA UDI

Identifiers

Catalog Number
4000120 FDA UDI
Primary DI / UDI-DI
00810042590052 FDA UDI
FDA Product Code
QIZ FDA UDI
QQQ FDA UDI
GMDN Term
Implantable intraocular medication reservoir FDA UDI

Classification

Device Class
N FDA UDI
Regulation Number
886.4300 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

No

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Implantable intraocular medication reservoir

Susvimo by Genentech, Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable intraocular medication reservoir.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Genentech, Inc.

Sources (1)

  • FDA UDI 82716127-09f5-4cc4-9646-43a068ce8349 35 fields · synced May 31, 2026