Identity
- Trade Name
- Susvimo FDA UDI
- Generic Name
- Ophthalmic implant handling forceps, single-use FDA UDI
- Device Name
- Susvimo Explant Tool FDA UDI
- Model / Reference
- 0580424 FDA UDI
- Description
- Susvimo Explant Tool FDA UDI
Identifiers
- Catalog Number
- 0580424 FDA UDI
- Primary DI / UDI-DI
- 00810042590038 FDA UDI
- GMDN Term
- Ophthalmic implant handling forceps, single-use FDA UDI
Classification
- Commercial Distribution
- 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
Yes
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
Yes
FDA UDI
Category: Ophthalmic implant handling forceps, single-use
Susvimo by Genentech, Inc. — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Genentech, Inc.
Sources (1)
- FDA UDI 9246db1a-d987-4083-97c6-1d6dbb531bfb 35 fields · synced May 31, 2026