FDA UDI In Commercial Distribution 🇺🇸 United States

ifit

DI: 00190746080944 · Model: 1952-22-016213HM · AMERICAN ORTHODONTICS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ifit
Primary DI
00190746080944
Version / Model
1952-22-016213HM
Catalog Number
1952-22-016213HM
Company Name
AMERICAN ORTHODONTICS CORPORATION
Labeler DUNS
044668515
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-22
Public Version
4
Public Version Date
2023-11-22
Public Version Status
Update
Public Device Record Key
14c73e81-c5d8-4f80-8f5c-c480c804664c

Device Description

DB TUBE IFIT MAX LEFT 2ND MOLAR 022 SLOT NON-CONV T-10 A=0 R5D W/HK MES

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DZD Tube, Orthodontic

GMDN Terms

Code Name
31759 Orthodontic tube

Identifiers

Type ID
Primary 00190746080944

Customer Contacts