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Key Surgical K-Wire Rack

FDA UDI

Class I (US FDA UDI)

by Key Surgical, LLC

Identity

Trade Name
Key Surgical K-Wire Rack FDA UDI
Generic Name
Orthopaedic bone pin container FDA UDI
Device Name
K-Wire Sterilization Rack, Holds 6 ea of 5 different diam 4-6-inch wire .028-inch - .062-inch FDA UDI
Model / Reference
KI-71-RACK-46 FDA UDI
Description
K-Wire Sterilization Rack, Holds 6 ea of 5 different diam 4-6-inch wire .028-inch - .062-inch FDA UDI

Identifiers

Primary DI / UDI-DI
00849771030652 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Orthopaedic bone pin container 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

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

Key Surgical K-Wire Rack by Key Surgical, LLC — 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
Key Surgical, LLC

Sources (1)

  • FDA UDI b73096af-3925-4f66-a0db-39a1fa31fa0d 35 fields · synced May 30, 2026