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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
Instrument tray, reusable FDA UDI
Device Name
IMPLANT SCOPE CONTAINER LID 450x70x70MM FDA UDI
Model / Reference
Y600.02 FDA UDI
Description
IMPLANT SCOPE CONTAINER LID 450x70x70MM FDA UDI

Identifiers

Primary DI / UDI-DI
B060Y600021 FDA UDI
510(k) Number
K131407 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

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: Instrument tray, reusable

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

Similar devices

Also classified as Instrument tray, 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 d7fcb05d-6129-4f6e-a67f-0930a051e133 35 fields · synced Jun 6, 2026