← Back to catalogue

Inion® Universal instruments

FDA UDI

Class I (US FDA UDI)

by Inion , Ltd.

Identity

Trade Name
Inion® Universal instruments FDA UDI
Generic Name
Thermoplastic-moulding water bath FDA UDI
Device Name
Inion Thermo (water bath 110 V + US plug) FDA UDI
Model / Reference
1 FDA UDI
Description
Inion Thermo (water bath 110 V + US plug) FDA UDI

Identifiers

Catalog Number
ACC-9804 FDA UDI
Primary DI / UDI-DI
06438408002106 FDA UDI
FDA Product Code
IRQ FDA UDI
GMDN Term
Thermoplastic-moulding water bath FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5950 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Thermoplastic-moulding water bath

Inion® Universal instruments by Inion , Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thermoplastic-moulding water bath.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Inion , Ltd.

Sources (1)

  • FDA UDI 4d3b2d8c-b98e-4ddb-8ee9-a5c925e197da 34 fields · synced May 30, 2026