FDA UDI In Commercial Distribution 🇺🇸 United States

EUROPA

DI: 10190886075692 · Model: SSEFL1717 · G & H Wire Company, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
EUROPA
Primary DI
10190886075692
Version / Model
SSEFL1717
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
2025-03-27
Public Version
1
Public Version Date
2025-04-04
Public Version Status
New
Public Device Record Key
a100a1f8-c012-49c0-8a66-65b2e8093157

Device Description

SS EUROPA I LWR .017x.017

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 00190886075695
Primary 10190886075692

Customer Contacts

Device Sizes

Type Value Unit Text
Width .017 Inch
Height .017 Inch