FDA UDI In Commercial Distribution 🇺🇸 United States

ADVANCE®

DI: 00192629271920 · Model: K0002011CN · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ADVANCE®
Primary DI
00192629271920
Version / Model
K0002011CN
Catalog Number
K0002011CN
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-28
Public Version
1
Public Version Date
2020-06-05
Public Version Status
New
Public Device Record Key
22f9085d-f874-4262-aa4f-75df912e097b

Device Description

ADVANCE® FIXATION PIN, HEADLES W/O GROOVE 80mm

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
No
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
62547 Intraoperative bone pin/screw, non-sterile

Identifiers

Type ID
Secondary M684K0002011CN1
Primary 00192629271920

Customer Contacts