← Back to catalogue

Memory Basket

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Memory Basket FDA UDI
Generic Name
Biliary/urinary stone retrieval basket, reusable FDA UDI
Device Name
Memory Hard Wire Basket FDA UDI
Model / Reference
G22002 FDA UDI
Description
Memory Hard Wire Basket FDA UDI

Identifiers

Catalog Number
MWB-2X4 FDA UDI
Primary DI / UDI-DI
00827002220027 FDA UDI
FDA Product Code
FFL FDA UDI
GMDN Term
Biliary/urinary stone retrieval basket, reusable 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

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

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, reusable

Memory Basket by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biliary/urinary stone retrieval basket, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 84ffe4e9-c950-4c10-9e51-d735aa9f34fa 36 fields · synced Jun 8, 2026