← Back to catalogue

Hexa Freeze

FDA UDI

Class II (US FDA UDI)

by Ecotec Manufacturing

Identity

Trade Name
Hexa Freeze FDA UDI
Generic Name
Cryogenic spray, dental FDA UDI
Device Name
Endo Freeze Spray FDA UDI
Model / Reference
HFE-0001 FDA UDI
Description
Endo Freeze Spray FDA UDI

Identifiers

Primary DI / UDI-DI
00752080000028 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
Not 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

Hexa Freeze by Ecotec Manufacturing — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Sources (1)

  • FDA UDI 45f54120-2b22-4f60-ae1f-c515da92b20f 35 fields · synced Jun 8, 2026