FDA UDI In Commercial Distribution 🇺🇸 United States

Flex

DI: 00850190004100 · Model: 25171 · MEDROBOTICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Flex
Primary DI
00850190004100
Version / Model
25171
Company Name
MEDROBOTICS CORPORATION
Labeler DUNS
002764627
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-01
Public Version
6
Public Version Date
2026-03-19
Public Version Status
Update
Public Device Record Key
a834dbc2-0994-44e2-8419-b2004f99362b

Device Description

Flex Rectoscope

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
FDF Colonoscope And Accessories, Flexible/Rigid

GMDN Terms

Code Name
38678 Robotic surgical telemanipulation system

Identifiers

Type ID
Primary 00850190004100