← Back to catalogue

Arctic Blast

FDA UDI

Class II (US FDA UDI)

by Marie Reiko Inc

Identity

Trade Name
Arctic Blast FDA UDI
Generic Name
Cryogenic spray, dental FDA UDI
Model / Reference
Arctic Blast FDA UDI

Identifiers

Primary DI / UDI-DI
D872AB100108 FDA UDI
FDA Product Code
EAT FDA UDI
GMDN Term
Cryogenic spray, dental FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1720 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cryogenic spray, dental

Arctic Blast by Marie Reiko Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryogenic spray, dental.

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
Marie Reiko Inc

Sources (1)

  • FDA UDI 483b86ca-2af6-4808-abe2-f76d74168aa5 32 fields · synced May 30, 2026