FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20887587029693 · Model: 292.801 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20887587029693
Version / Model
292.801
Catalog Number
292801
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2015-09-14
Public Version
5
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
464a365a-f070-49eb-8f10-e154c01ebe38

Device Description

2.0MM KIRSCHNER WIRE W/CALIB W/15MM THRD-TROCAR POINT-150MM

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
DZL SCREW, FIXATION, INTRAOSSEOUS

GMDN Terms

Code Name
47635 Implantable craniofacial bone distractor

Identifiers

Type ID
Primary 20887587029693
Unit of Use 80887587029695
Secondary H9802928010

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K981362 000