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Container for Kit

FDA UDI

Class I (US FDA UDI)

by Etgar - Medical Instruments Ltd

Identity

Trade Name
Container for Kit FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Large Metal Sterilization Container FDA UDI
Model / Reference
EK-0410 FDA UDI
Description
Large Metal Sterilization Container FDA UDI

Identifiers

Primary DI / UDI-DI
07290112448644 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Device sterilization/disinfection container, reusable

Container for Kit by Etgar - Medical Instruments Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 20a8714f-4f20-4899-a0ec-9967ab5e40f6 33 fields · synced May 30, 2026