FDA UDI In Commercial Distribution 🇺🇸 United States

FLEX

DI: 00850190004933 · Model: Instrument Assembly part · MEDROBOTICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FLEX
Primary DI
00850190004933
Version / Model
Instrument Assembly part
Company Name
MEDROBOTICS CORPORATION
Labeler DUNS
002764627
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-18
Public Version
5
Public Version Date
2023-06-19
Public Version Status
Update
Public Device Record Key
83facc91-5b21-4fa3-b57d-12d6175d77a5

Device Description

Clamp

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EOB Nasopharyngoscope (Flexible Or Rigid)

GMDN Terms

Code Name
38678 Robotic surgical arm system

Identifiers

Type ID
Primary 00850190004933