← Back to catalogue

Axiom Generator

FDA UDI

Class II (US FDA UDI)

by Peter Brasseler Holdings, LLC

Identity

Trade Name
Axiom Generator FDA UDI
Generic Name
Hard/soft-tissue ultrasonic surgical system FDA UDI
Device Name
BRAXM-UG FDA UDI
Model / Reference
BRAXM-UG FDA UDI
Description
BRAXM-UG FDA UDI

Identifiers

Primary DI / UDI-DI
08404535016413 FDA UDI
FDA Product Code
LZV FDA UDI
GMDN Term
Hard/soft-tissue ultrasonic surgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.4580 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Hard/soft-tissue ultrasonic surgical system

Axiom Generator by Peter Brasseler Holdings, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hard/soft-tissue ultrasonic surgical system.

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 5af7e33d-7c6b-4c61-a1b2-d875b53f72bd 33 fields · synced Jun 6, 2026