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NIDO Pedicle Screw System

FDA UDI

Class I (US FDA UDI)

by Kalitec Direct LLC

Identity

Trade Name
NIDO Pedicle Screw System FDA UDI
Generic Name
Surgical instrument/implant rack FDA UDI
Device Name
Caddie, Locking Caps FDA UDI
Model / Reference
15-K01-0044 FDA UDI
Description
Caddie, Locking Caps FDA UDI

Identifiers

Catalog Number
15-K01-0044 FDA UDI
Primary DI / UDI-DI
B07315K0100440 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
Surgical instrument/implant rack 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

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

No

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: Surgical instrument/implant rack

NIDO Pedicle Screw System by Kalitec Direct LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument/implant rack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kalitec Direct LLC

Sources (1)

  • FDA UDI 0419c813-56b6-4b58-b72c-02676d0862ba 34 fields · synced May 30, 2026