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Scheker DRUJ

FDA UDI

Class I (US FDA UDI)

by Aptis Medical, Llc.

Identity

Trade Name
Scheker DRUJ FDA UDI
Generic Name
Orthopaedic bone pin, non-bioabsorbable FDA UDI
Device Name
K-Wire D. TROCAR .054" FDA UDI
Model / Reference
DRUJ-KW54 FDA UDI
Description
K-Wire D. TROCAR .054" FDA UDI

Identifiers

Catalog Number
DRUJ-KW54 FDA UDI
Primary DI / UDI-DI
B013DRUJKW540 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable 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

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic bone pin, non-bioabsorbable

Scheker DRUJ by Aptis Medical, Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aptis Medical, Llc.

Sources (1)

  • FDA UDI 4f855f93-7994-4c4b-bf4d-e247e0ed9073 34 fields · synced Jun 8, 2026