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532nm VITRA MULTISPOT adaptor for OPTIMIS FUSION coupling

FDA UDI

Class II (US FDA UDI)

by Quantel Medical

Identity

Trade Name
532nm VITRA MULTISPOT adaptor for OPTIMIS FUSION coupling FDA UDI
Generic Name
Laser adaptor FDA UDI
Model / Reference
VMSSC532FUS FDA UDI

Identifiers

Catalog Number
1 FDA UDI
Primary DI / UDI-DI
03700542625446 FDA UDI
FDA Product Code
HQF FDA UDI
GMDN Term
Laser adaptor 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

No

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: Laser adaptor

The 532nm VITRA MULTISPOT adaptor for OPTIMIS FUSION coupling is a reusable, implantable device designed to join lasers and fibreoptic laser delivery systems. It features a single-use model with serial numbering and is exempt from PM exemption and OTC labeling requirements.

Similar devices

Also classified as Laser adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quantel Medical

Sources (1)

  • FDA UDI e032a891-7330-460f-a1e9-e7f7a801a401 34 fields · synced Jun 20, 2026