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Needle Guide Bracket Kit

FDA UDI

Class II (US FDA UDI)

by Edan Instruments, Inc.

Identity

Trade Name
Needle Guide Bracket Kit FDA UDI
Generic Name
Ultrasound imaging system tracking positioner, reusable FDA UDI
Model / Reference
BGK-006 FDA UDI

Identifiers

Primary DI / UDI-DI
06944413811782 FDA UDI
510(k) Number
K192879 FDA UDI
K250214 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Ultrasound imaging system tracking positioner, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Ultrasound imaging system tracking positioner, reusable

Needle Guide Bracket Kit by Edan Instruments, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasound imaging system tracking positioner, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 51dc9f8b-93fb-4eb3-b9dd-634724cd7cf9 33 fields · synced Jun 1, 2026