GUDIDData
gudid Primary ID: P63-21W-2040-01

ApeTape (UDI P63-21W-2040-01)

Manufactured by RIVERPOINT MEDICAL, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ApeTape - Primary ID P63-21W-2040-01

Device Regulatory Overview

The ApeTape (Model/Catalog Number: P63-21W-2040-01) is a medical device manufactured by RIVERPOINT MEDICAL, LLC. This product is indexed under FDA Product Code / Category Classification GAT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
P63-21W-2040-01
Product Code / EMDN
GAT
Device Name
White/Black UHMWPE Non-Absorbable Suture Tape
Database Sync Date
2026-08-09 09:12:05

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of ApeTape?

The registered manufacturer of record for ApeTape is RIVERPOINT MEDICAL, LLC.

What is the Primary UDI-DI identifier for ApeTape?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is P63-21W-2040-01.

What classification code is assigned to this device?

This device is registered under product classification code GAT.

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