FDA UDI In Commercial Distribution 🇺🇸 United States

Single use Surgical Optical Fiber

DI: 08033945934453 · Model: OAF402011 · QUANTA SYSTEM SPA
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Single use Surgical Optical Fiber
Primary DI
08033945934453
Version / Model
OAF402011
Company Name
QUANTA SYSTEM SPA
Labeler DUNS
436045833
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-29
Public Version
6
Public Version Date
2022-10-24
Public Version Status
Update
Public Device Record Key
55b42410-42b9-462a-9e2a-490531a56599

Device Description

Single use Surgical Optical Fiber Ø 200 µm

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
47785 Urogenital surgical laser system beam guide, single-use

Identifiers

Type ID
Primary 08033945934453
Package 08033945935467
Package 8033945935610