FDA UDI In Commercial Distribution 🇺🇸 United States

Thuvera

DI: 00810071230837 · Model: MD2100F-001632R · IPG Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Thuvera
Primary DI
00810071230837
Version / Model
MD2100F-001632R
Company Name
IPG Medical Corporation
Labeler DUNS
081504133
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-05
Public Version
1
Public Version Date
2024-12-13
Public Version Status
New
Public Device Record Key
4f986654-5fc2-4bf1-9cc5-e74944e9eede

Device Description

Thuvera Thulium Fiber Laser System - Repair

Device Characteristics

Single Use
Yes
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

GMDN Terms

Code Name
36170 General/multiple surgical solid-state laser system

Identifiers

Type ID
Primary 00810071230837

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
20 – 75 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius