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Mistral-Air

FDA UDI

Class II (US FDA UDI)

by The Surgical Company International B.V.

Identity

Trade Name
Mistral-Air FDA UDI
Generic Name
Utility trolley FDA UDI
Device Name
MA1200 Trolley - SYK FDA UDI
Model / Reference
MA5250-PM FDA UDI
Description
MA1200 Trolley - SYK FDA UDI

Identifiers

Primary DI / UDI-DI
ET37MA5250PM0 FDA UDI
FDA Product Code
DWJ FDA UDI
GMDN Term
Utility trolley FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5900 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Utility trolley

Mistral-Air by The Surgical Company International B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Utility trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
The Surgical Company International B.V.

Sources (1)

  • FDA UDI 4c03c4c9-6ff8-4725-a8d7-7fc7a61a0b74 34 fields · synced Jun 1, 2026