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Standop Volista®

FDA UDI

Class II (US FDA UDI)

by Maquet, Inc.

Identity

Trade Name
STANDOP VOLISTA® FDA UDI
Generic Name
Operating room light FDA UDI
Device Name
SAT VST60DF 12 FDA UDI
Model / Reference
ARDSAT209034A FDA UDI
Description
SAT VST60DF 12 FDA UDI

Identifiers

Primary DI / UDI-DI
03700712405649 FDA UDI
FDA Product Code
FTD FDA UDI
FSY FDA UDI
GMDN Term
Operating room light FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Standop Volista® by Maquet, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maquet, Inc.

Sources (1)

  • FDA UDI ef7ef15a-5ee8-4a44-b156-5fa46acd3e75 34 fields · synced May 31, 2026