FDA UDI In Commercial Distribution 🇺🇸 United States

EUROPA

DI: 10190886256107 · Model: SEEFU3925ACB · G & H Wire Company, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
EUROPA
Primary DI
10190886256107
Version / Model
SEEFU3925ACB
Company Name
G & H Wire Company, Inc.
Labeler DUNS
831465641
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2025-03-26
Public Version
1
Public Version Date
2025-04-03
Public Version Status
New
Public Device Record Key
64d8ad10-989e-4ba7-9d5d-681b3db51ef4

Device Description

SE NITI EUROPA II UPR 019x025 W/STPS

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
DZC WIRE, ORTHODONTIC

GMDN Terms

Code Name
41397 Orthodontic archwire

Identifiers

Type ID
Unit of Use 00190886256100
Primary 10190886256107

Customer Contacts

Device Sizes

Type Value Unit Text
Width .025 Inch
Height .019 Inch