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Mistral-Air® Premium Lithotomy

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MA3455Model MA0510

by The Surgical Company International B.V.

Identity

Trade Name
Mistral-Air® Premium Lithotomy EUDAMED
Mistral-Air FDA UDI
Generic Name
External circulating-air core temperature regulation system pad, single-use FDA UDI
Device Name
Mistral-Air® Tube EUDAMED
Mistral-Air® Premium Lithotomy FDA UDI
Model / Reference
MA0510 EUDAMED
MA3455 EUDAMEDFDA UDI
Description
Mistral-Air® Premium Lithotomy FDA UDI

Identifiers

Primary DI / UDI-DI
08719867002653 EUDAMEDFDA UDI
Basic UDI-DI
8719867EMDNT030301KX EUDAMED
FDA Product Code
DWJ FDA UDI
EMDN Code
T030301 AIR FLOW BLANKETS EUDAMED
GMDN Term
External circulating-air core temperature regulation system pad, single-use FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
870.5900 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Mistral-Air® Premium Lithotomy by The Surgical Company International B.V. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
NL-MF-000001973

Sources (2)

  • EUDAMED c9cae631-63ef-42f7-b304-be41fd4550ff 61 fields · synced Oct 6, 2026
  • FDA UDI f28fc21e-f2b3-4edf-b4db-828ebbe9c276 33 fields · synced May 30, 2026