FDA UDI In Commercial Distribution 🇺🇸 United States

GRYPHON Flex

DI: 10886705032518 · Model: 208960 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
GRYPHON Flex
Primary DI
10886705032518
Version / Model
208960
Catalog Number
208960
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-17
Public Version
1
Public Version Date
2024-05-27
Public Version Status
New
Public Device Record Key
b4d60685-690e-4bff-b361-af141a034192

Device Description

GRYPHON Flex Knotless Anchor Sawtooth Curved Guide

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
No

Product Codes

Code Name
FZX Guide, surgical, instrument

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 10886705032518

Customer Contacts