FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10887587015293 · Model: 04.307.001 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10887587015293
Version / Model
04.307.001
Catalog Number
04307001
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-14
Public Version
6
Public Version Date
2023-01-16
Public Version Status
Update
Public Device Record Key
944ce047-418f-4d5d-954d-a7cc2a438b71

Device Description

TI MAXILLARY FOOTPLATE 40MM

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
MQN EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

GMDN Terms

Code Name
47636 Craniofacial bone distractor extension

Identifiers

Type ID
Secondary H980043070010
Primary 10887587015293

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K040083 000