← Back to catalogue

Wizard Wand

FDA UDI

Class I (US FDA UDI)

by C F M Technologies Inc

Identity

Trade Name
Wizard Wand FDA UDI
Generic Name
Corneal staining strip FDA UDI
Device Name
Wizard Wand Professional Eye Care Set. This kit contains a versatile set of components designed to facilitate effective examination of the eyes for foreign bodies and corneal abrasions and removal of foreign bodies from the conjunctiva. FDA UDI
Model / Reference
WW-01 FDA UDI
Description
Wizard Wand Professional Eye Care Set. This kit contains a versatile set of components designed to facilitate effective examination of the eyes for foreign bodies and corneal abrasions and removal of foreign bodies from the conjunctiva. FDA UDI

Identifiers

Primary DI / UDI-DI
00850013958122 FDA UDI
FDA Product Code
HPN FDA UDI
GMDN Term
Corneal staining strip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4445 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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ENT diagnostic setEye magnet, non-poweredCorneal staining strip

Wizard Wand by C F M Technologies Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Corneal staining strip.

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
C F M Technologies Inc

Sources (1)

  • FDA UDI eda3964d-1fa3-4b89-ae08-01d990800a3b 34 fields · synced May 30, 2026