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Grappler Interference Screw System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Grappler Interference Screw System FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
PCFD Tether, System Tray FDA UDI
Model / Reference
P62-CAD-0001 FDA UDI
Description
PCFD Tether, System Tray FDA UDI

Identifiers

Catalog Number
P62-CAD-0001 FDA UDI
Primary DI / UDI-DI
00889795141538 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Device sterilization/disinfection container, reusable

Grappler Interference Screw System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI a96ab7e7-2056-4381-be99-724c26de86a9 34 fields · synced May 31, 2026