Identity
- Trade Name
- Synergetics FDA UDI
- Generic Name
- General-purpose ophthalmic hook, single-use FDA UDI
- Device Name
- Stiff 25ga Tano Diamond Dusted Membrane Scraper (DDMS™) FDA UDI
- Model / Reference
- 20.04.25S FDA UDI
- Description
- Stiff 25ga Tano Diamond Dusted Membrane Scraper (DDMS™) FDA UDI
Identifiers
- Catalog Number
- 20.04.25S FDA UDI
- Primary DI / UDI-DI
- 20841305108848 FDA UDI
- FDA Product Code
- GZX FDA UDI
- GMDN Term
- General-purpose ophthalmic hook, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 FDA UDI
- 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
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General-purpose ophthalmic hook, single-use
Synergetics by Synergetics Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as General-purpose ophthalmic hook, single-use.
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- 20GA Membrane Scraper — Peregrine Surgical, LLC. · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Synergetics Usa, Inc.
Sources (1)
- FDA UDI 6fc5fcb7-8cf6-4080-9847-17e89c258781 35 fields · synced May 30, 2026