gudid Primary ID: 60.612.035

Tube 5ml, 92x15.3 (rund), PP (UDI 60.612.035)

Manufactured by Sarstedt Aktiengesellschaft & Co.KG

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Tube 5ml, 92x15.3 (rund), PP (Model/Catalog Number: 60.612.035) is a medical device manufactured by Sarstedt Aktiengesellschaft & Co.KG. This product is indexed under FDA Product Code / Category Classification NNK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 60.612.035
Product Code / EMDN: NNK
Device Name
Database Sync Date: 2026-08-09 09:46:24

Full Regulatory Attributes

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{
    "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 Tube 5ml, 92x15.3 (rund), PP?

The registered manufacturer of record for Tube 5ml, 92x15.3 (rund), PP is Sarstedt Aktiengesellschaft & Co.KG.

What is the Primary UDI-DI identifier for Tube 5ml, 92x15.3 (rund), PP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 60.612.035.

What classification code is assigned to this device?

This device is registered under product classification code NNK.

Similar Classification Devices (NNK)

Other Devices by Sarstedt Aktiengesellschaft & Co.KG

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