FDA UDI In Commercial Distribution 🇺🇸 United States

Surgical Instrument

DI: 08800089476459 · Model: 111-497 · Jeil Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgical Instrument
Primary DI
08800089476459
Version / Model
111-497
Company Name
Jeil Medical Corporation
Labeler DUNS
688811603
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-03
Public Version
1
Public Version Date
2025-07-11
Public Version Status
New
Public Device Record Key
659e9e30-6dad-4715-8d4f-205b0c15534e

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
Yes
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
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 08800089476459