FDA UDI In Commercial Distribution 🇺🇸 United States

SUPERPATH®

DI: 00192629260825 · Model: 2007XL12 · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SUPERPATH®
Primary DI
00192629260825
Version / Model
2007XL12
Catalog Number
2007XL12
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
1
Public Version Date
2021-04-16
Public Version Status
New
Public Device Record Key
a03cbc06-b4ef-4e7c-a601-71f241164e4e

Device Characteristics

Single Use
No
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
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
35095 Surgical drill guide, reusable

Identifiers

Type ID
Secondary M6842007XL121
Primary 00192629260825

Customer Contacts