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Bahadir Usa

FDA UDI

Class II (US FDA UDI)

by Bahadir Usa Llc

Identity

Trade Name
BAHADIR USA FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
MINI BOTTOM NON PERFORATED 300X140X70MM FDA UDI
Model / Reference
Y405.07A FDA UDI
Description
MINI BOTTOM NON PERFORATED 300X140X70MM FDA UDI

Identifiers

Primary DI / UDI-DI
00859982006698 FDA UDI
510(k) Number
K131407 FDA UDI
FDA Product Code
KCT FDA UDI
GMDN Term
Device sterilization/disinfection container, 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Device sterilization/disinfection container, reusable

Bahadir Usa by Bahadir Usa Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bahadir Usa Llc

Sources (1)

  • FDA UDI 3cef8998-f4df-45d6-87e7-5bffa9c7850b 35 fields · synced May 31, 2026