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Stone Extraction Baskets

FDA UDI

Class II (US FDA UDI)

by Changzhou Health Microport Medical Device Co., Ltd

Identity

Trade Name
Stone Extraction Baskets FDA UDI
Generic Name
Biliary/urinary stone retrieval basket, single-use FDA UDI
Model / Reference
HM/113-2.4/1800 FDA UDI

Identifiers

Primary DI / UDI-DI
06951862236660 FDA UDI
FDA Product Code
FFL FDA UDI
GMDN Term
Biliary/urinary stone retrieval basket, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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: Biliary/urinary stone retrieval basket, single-use

Stone Extraction Baskets by Changzhou Health Microport Medical Device Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biliary/urinary stone retrieval basket, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0c9df804-5e93-47f7-8783-5db50c1ec724 32 fields · synced May 30, 2026