FDA UDI In Commercial Distribution 🇺🇸 United States

GRYPHON

DI: 10886705027576 · Model: 219102 · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GRYPHON
Primary DI
10886705027576
Version / Model
219102
Catalog Number
219102
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-22
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
951b898b-451e-4407-8d1d-ac5d1a960b7f

Device Description

GRYPHON Cannulated Hip Obturator

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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
33997 Surgical drill guide obturator

Identifiers

Type ID
Primary 10886705027576

Customer Contacts