FDA UDI In Commercial Distribution 🇺🇸 United States

SUPERPATH®

DI: 00192629260818 · Model: 2007XL07 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SUPERPATH®
Primary DI
00192629260818
Version / Model
2007XL07
Catalog Number
2007XL07
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-04-08
Public Version
2
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
02de7e72-127a-44ff-a1c1-299f359ab9d3

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
No
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
HTW BIT, DRILL

GMDN Terms

Code Name
47863 Surgical instrument/implant depth limiter

Identifiers

Type ID
Secondary M6842007XL071
Primary 00192629260818

Customer Contacts