FDA UDI In Commercial Distribution 🇺🇸 United States

N.A.

DI: J011402253000 · Model: 402-253-00 · DENTAURUM GmbH & Co.KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N.A.
Primary DI
J011402253000
Version / Model
402-253-00
Company Name
DENTAURUM GmbH & Co.KG
Labeler DUNS
315427286
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
1a93bac8-119a-411d-b150-b52a89a214ed

Device Description

Jaw fracture splint

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EHO BAR, PREFORMED

GMDN Terms

Code Name
16204 Orthodontic wire

Identifiers

Type ID
Primary J011402253000

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
No special storage conditions required