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Surfix®

FDA UDI

Class I (US FDA UDI)

by Newdeal Sas

Identity

Trade Name
SURFIX® FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
This K-Wire of diameter 2.5 mm and of length 250 mm is used to guide the instrumentation and the screws. FDA UDI
Model / Reference
529061ND FDA UDI
Description
This K-Wire of diameter 2.5 mm and of length 250 mm is used to guide the instrumentation and the screws. FDA UDI

Identifiers

Primary DI / UDI-DI
10381780043256 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic guidewire, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Orthopaedic guidewire, single-use

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

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Newdeal Sas

Sources (1)

  • FDA UDI c949f249-6eb4-48bb-bc7c-8837729bdd7c 37 fields · synced May 30, 2026