FDA UDI In Commercial Distribution 🇺🇸 United States

Preformed Ligature Wire

DI: D90927001815 · Model: 270-018 · Ortho Arch Company Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Preformed Ligature Wire
Primary DI
D90927001815
Version / Model
270-018
Catalog Number
270-018
Company Name
Ortho Arch Company Inc
Labeler DUNS
020956330
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-02
Public Version
1
Public Version Date
2022-02-10
Public Version Status
New
Public Device Record Key
7eaebb2a-8674-4cce-8a4d-184a658d175f

Device Description

.012 TOOTHTONE PREFORMED LIGATURE WIRE (100)

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
ECP Instrument, Ligature Tucking, Orthodontic

GMDN Terms

Code Name
41677 Orthodontic archwire/bracket ligature

Identifiers

Type ID
Primary D90927001815