FDA UDI In Commercial Distribution 🇺🇸 United States

Tigon Medical

DI: 00854288008261 · Model: TIGO PRO 001 · Tigon Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tigon Medical
Primary DI
00854288008261
Version / Model
TIGO PRO 001
Company Name
Tigon Medical LLC
Labeler DUNS
080929031
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-18
Public Version
1
Public Version Date
2025-08-26
Public Version Status
New
Public Device Record Key
de28ed52-c755-4f5e-90f7-f50099a206e3

Device Description

Arthroscopic Knot Pusher

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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
45716 Suture knot pusher, reusable

Identifiers

Type ID
Primary 00854288008261