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Kidney Stone Collection Kit

FDA UDI

Class I (US FDA UDI)

by Ditek Consulting Llc

Identity

Trade Name
Kidney Stone Collection Kit FDA UDI
Generic Name
General specimen receptacle transport container FDA UDI
Device Name
Kidney Stone Collection Kit (146225) FDA UDI
Model / Reference
146225 FDA UDI
Description
Kidney Stone Collection Kit (146225) FDA UDI

Identifiers

Primary DI / UDI-DI
00860011770282 FDA UDI
FDA Product Code
OIB FDA UDI
GMDN Term
General specimen receptacle transport container FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General specimen receptacle transport container

Kidney Stone Collection Kit by Ditek Consulting Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen receptacle transport container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ditek Consulting Llc

Sources (1)

  • FDA UDI 650476ba-66a3-4898-87b3-7e6e1ac69b1a 33 fields · synced May 30, 2026