GUDIDData
gudid Primary ID: STOCKMAN (ZIPSER) PENIS CLAMP

PENIS CLAMP (UDI STOCKMAN (ZIPSER) PENIS CLAMP)

Manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PENIS CLAMP - Primary ID STOCKMAN (ZIPSER) PENIS CLAMP

Device Regulatory Overview

The PENIS CLAMP (Model/Catalog Number: STOCKMAN (ZIPSER) PENIS CLAMP) is a medical device manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,. This product is indexed under FDA Product Code / Category Classification FHA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
STOCKMAN (ZIPSER) PENIS CLAMP
Product Code / EMDN
FHA
Device Name
STOCKMAN (ZIPSER) PENIS CLAMP 5.5 INCH
Database Sync Date
2026-08-09 09:06:20

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of PENIS CLAMP?

The registered manufacturer of record for PENIS CLAMP is DR.FRIGZ INTERNATIONAL(PVT)LTD,.

What is the Primary UDI-DI identifier for PENIS CLAMP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is STOCKMAN (ZIPSER) PENIS CLAMP.

What classification code is assigned to this device?

This device is registered under product classification code FHA.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint