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Brasseler USA

FDA UDI

Class II (US FDA UDI)

by Peter Brasseler Holdings, LLC

Identity

Trade Name
Brasseler USA FDA UDI
Generic Name
Cryogenic spray, dental FDA UDI
Device Name
PULP VITALITY SPRAY 1P FDA UDI
Model / Reference
5026551U0 FDA UDI
Description
PULP VITALITY SPRAY 1P FDA UDI

Identifiers

Primary DI / UDI-DI
00887919807193 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cryogenic spray, dental

Brasseler USA by Peter Brasseler Holdings, LLC — 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

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Manufacturer

Sources (1)

  • FDA UDI ac072745-f8e6-476f-bc24-76b671f92f61 33 fields · synced May 30, 2026