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Synergetics

FDA UDI

Class I (US FDA UDI)

by Synergetics Usa, Inc.

Identity

Trade Name
Synergetics FDA UDI
Generic Name
General-purpose ophthalmic hook, single-use FDA UDI
Device Name
23ga Tano Diamond Dusted Membrane Scraper (DDMS™) FDA UDI
Model / Reference
20.04.23 FDA UDI
Description
23ga Tano Diamond Dusted Membrane Scraper (DDMS™) FDA UDI

Identifiers

Catalog Number
20.04.23 FDA UDI
Primary DI / UDI-DI
20841305108831 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

Similar devices

Also classified as General-purpose ophthalmic hook, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d108bece-f0e6-49b0-8811-cecf8ebbcc3c 35 fields · synced May 30, 2026