Hnm Medical

FDA UDI

Class II (US FDA UDI)

by Hnm Stainless, Llc.

Identity

Trade Name: HNM MEDICAL FDA UDI
Generic Name: Instrument tray, reusable FDA UDI
Device Name: STERILIZATION CONTAINER, BOTTOM NON PERFORATED, 22 7/8"X11X5 3/8", W/LID, SAFE FDA UDI
Model / Reference: HNM-112.13W FDA UDI
Description: STERILIZATION CONTAINER, BOTTOM NON PERFORATED, 22 7/8"X11X5 3/8", W/LID, SAFE FDA UDI

Identifiers

Catalog Number: HNM-112.103W FDA UDI
Primary DI / UDI-DI: 00842962152836 FDA UDI
FDA Product Code: KCT FDA UDI
GMDN Term: Instrument tray, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6850 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

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Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Instrument tray, reusable

A comprehensive and detailed description of the device in clear, natural language. The purpose is to inform users about its features, usage, and benefits.

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Hnm Stainless, Llc.

Sources (1)

FDA UDI 9cf3baba-c3f2-41a7-a34b-00f6c7649541 34 fields · synced Jul 17, 2026