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Synergetics

FDA UDI

Class II (US FDA UDI)

by Synergetics Usa, Inc.

Identity

Trade Name
Synergetics FDA UDI
Generic Name
Ophthalmic light source FDA UDI
Device Name
Synerfit™ Single Fiber Adapter for Bausch & Lomb Stellaris FDA UDI
Model / Reference
57.40 FDA UDI
Description
Synerfit™ Single Fiber Adapter for Bausch & Lomb Stellaris FDA UDI

Identifiers

Catalog Number
57.40 FDA UDI
Primary DI / UDI-DI
10841305111513 FDA UDI
FDA Product Code
ONE FDA UDI
GMDN Term
Ophthalmic light source FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic light source

Synergetics by Synergetics Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic light source.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synergetics Usa, Inc.

Sources (1)

  • FDA UDI 0845e5f3-a456-4b52-9948-0e9654407462 35 fields · synced May 30, 2026