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Scan attachable delivery unit (SL130)

FDA UDI

Class II (US FDA UDI)

by Nidek, Inc.

Identity

Trade Name
Scan attachable delivery unit (SL130) FDA UDI
Generic Name
General/multiple surgical frequency-doubled solid-state laser system FDA UDI
Device Name
The scan attachable delivery unit is mainly comprised of a photocoagulation unit and a protective filter unit. They are attached to the Carl Zeiss Meditec SL 130 (Zeiss SL 130) to comprise a scan slit lamp delivery unit. The comprised scan slit lamp delivery unit is connected to the NIDEK Multicolor Laser Photocoagulator, Model MC-500 to comprise a photocoagulation system. The photocoagulation system allows the operator to select among photocoagulation with the red (647 nm), yellow (577 nm), or green (532 nm) laser beam and observation of the affected area with the slit lamp. FDA UDI
Model / Reference
17467-0000 FDA UDI
Description
The scan attachable delivery unit is mainly comprised of a photocoagulation unit and a protective filter unit. They are attached to the Carl Zeiss Meditec SL 130 (Zeiss SL 130) to comprise a scan slit lamp delivery unit. The comprised scan slit lamp delivery unit is connected to the NIDEK Multicolor Laser Photocoagulator, Model MC-500 to comprise a photocoagulation system. The photocoagulation system allows the operator to select among photocoagulation with the red (647 nm), yellow (577 nm), or green (532 nm) laser beam and observation of the affected area with the slit lamp. FDA UDI

Identifiers

Primary DI / UDI-DI
04987669100172 FDA UDI
FDA Product Code
HQF FDA UDI
GMDN Term
General/multiple surgical frequency-doubled solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General/multiple surgical frequency-doubled solid-state laser system

Scan attachable delivery unit (SL130) by Nidek, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General/multiple surgical frequency-doubled solid-state laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nidek, Inc.

Sources (1)

  • FDA UDI 81297154-775f-41bc-a6b3-53270328ec97 34 fields · synced May 30, 2026