FDA UDI In Commercial Distribution 🇺🇸 United States

SegWAY

DI: 00857356008200 · Model: 200-1009 · TRICE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SegWAY
Primary DI
00857356008200
Version / Model
200-1009
Company Name
TRICE MEDICAL, INC.
Labeler DUNS
009452895
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
4077c500-acd7-46fa-afcf-1f4c0998edfe

Device Description

Short Retrograde Ligament Knife

Device Characteristics

Single Use
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
47569 Scalpel, single-use

Identifiers

Type ID
Primary 00857356008200