FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 08809974445259 · Model: SC7TR1612 · Medyssey Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
08809974445259
Version / Model
SC7TR1612
Company Name
Medyssey Co., Ltd.
Labeler DUNS
688211503
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-11
Public Version
2
Public Version Date
2025-04-03
Public Version Status
Update
Public Device Record Key
3fca6a0a-acc6-41db-8b1e-e7cb41de1634
Distribution End Date
2025-04-03

Device Description

C7 TRIAL RASP Lordotic6° (W12xL14xH16)

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
35559 Bone file/rasp, manual, reusable

Identifiers

Type ID
Primary 08809974445259