FDA UDI In Commercial Distribution 🇺🇸 United States

Exodus Revision

DI: 00850019455052 · Model: 00-507-400-17 · Tightline Development, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Exodus Revision
Primary DI
00850019455052
Version / Model
00-507-400-17
Company Name
Tightline Development, LLC
Labeler DUNS
116512702
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-21
Public Version
1
Public Version Date
2023-07-31
Public Version Status
New
Public Device Record Key
e89ca327-3565-4fe0-b2e4-b7777e48469e

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
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
12844 Orthopaedic osteotome

Identifiers

Type ID
Primary 00850019455052