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Hallu®-FIX

FDA UDI

Class I (US FDA UDI)

by Newdeal Sas

Identity

Trade Name
Hallu®-FIX FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
The radel plate tray is part of the container with reference 129930ND used in the transport and the sterilization of the HALLU®-C associated instruments and non sterile implants. It has one silicone bumper to securely maintain the HALLU®-C plates. The transport and sterilization containers are not intended to maintain sterility. FDA UDI
Model / Reference
129932ND FDA UDI
Description
The radel plate tray is part of the container with reference 129930ND used in the transport and the sterilization of the HALLU®-C associated instruments and non sterile implants. It has one silicone bumper to securely maintain the HALLU®-C plates. The transport and sterilization containers are not intended to maintain sterility. FDA UDI

Identifiers

Primary DI / UDI-DI
10381780042112 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Hallu®-FIX by Newdeal Sas — Class I — 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
Newdeal Sas

Sources (1)

  • FDA UDI 6f707d43-4eaf-49e6-96fc-53e833ad30c5 35 fields · synced May 30, 2026