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Quick Spherz

FDA UDI

Class II (US FDA UDI)

by Izi Medical Products Llc

Identity

Trade Name
Quick Spherz FDA UDI
Generic Name
Radiographic image marker, manual FDA UDI
Model / Reference
2021-120 FDA UDI

Identifiers

Primary DI / UDI-DI
00815212021626 FDA UDI
510(k) Number
K022074 FDA UDI
FDA Product Code
HAW FDA UDI
GMDN Term
Radiographic image marker, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiographic image marker, manual

Quick Spherz by Izi Medical Products Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiographic image marker, manual.

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 a584d372-60f3-482f-8cb3-80af4136211a 33 fields · synced Jun 1, 2026