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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
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
The radel quick coupling system is used to allow the engagement of the various metatarsal and phalangeal reamers with 6.0mm diameter tri shank attachments, over the 1.6mm K-wires, for motor power reaming. FDA UDI
Model / Reference
129710ND FDA UDI
Description
The radel quick coupling system is used to allow the engagement of the various metatarsal and phalangeal reamers with 6.0mm diameter tri shank attachments, over the 1.6mm K-wires, for motor power reaming. FDA UDI

Identifiers

Primary DI / UDI-DI
10381780051435 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument handle, non-torque-limiting

Hallu®-FIX by Newdeal Sas — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Newdeal Sas

Sources (1)

  • FDA UDI d0d0cc19-7b6f-4686-91db-ccf2b5d33a2c 35 fields · synced May 31, 2026