GUDIDData
eudamed_udi Primary ID: 08902895692129

Peters (UDI 08902895692129)

Manufactured by Aditya Dispomed Products Pvt. Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Peters - Primary ID 08902895692129

Device Regulatory Overview

The Peters (Model/Catalog Number: T69212) is a medical device manufactured by Aditya Dispomed Products Pvt. Ltd.. This product is indexed under FDA Product Code / Category Classification V010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
T69212
Product Code / EMDN
V010102
Device Name
Disposable Scalpel
Database Sync Date
2026-08-09 16:46:28

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 Peters?

The registered manufacturer of record for Peters is Aditya Dispomed Products Pvt. Ltd..

What is the Primary UDI-DI identifier for Peters?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08902895692129.

What classification code is assigned to this device?

This device is registered under product classification code V010102.

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