FDA UDI In Commercial Distribution 🇺🇸 United States

Regenalase

DI: 00810071230509 · Model: MD2300F-001780 · IPG Medical Corporation
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Regenalase
Primary DI
00810071230509
Version / Model
MD2300F-001780
Company Name
IPG Medical Corporation
Labeler DUNS
081504133
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-09
Public Version
1
Public Version Date
2025-06-17
Public Version Status
New
Public Device Record Key
b8796a57-1050-46cf-ba08-b9792513cfa9

Device Description

Laser System

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument
ILY Lamp, Infrared, Therapeutic Heating

GMDN Terms

Code Name
60341 General/multiple surgical diode laser system
60409 Musculoskeletal/physical therapy laser, professional

Identifiers

Type ID
Primary 00810071230509