FDA UDI In Commercial Distribution 🇺🇸 United States

EUROPA SOLO-PACK

DI: 10190886215890 · Model: TEFU3425AS · G & H Wire Company, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
EUROPA SOLO-PACK
Primary DI
10190886215890
Version / Model
TEFU3425AS
Company Name
G & H Wire Company, Inc.
Labeler DUNS
831465641
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
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
115deafd-cdac-45e8-941f-b0639be480fa

Device Description

TH NITI EUROPA II UPR .014x.025 SOLO-PACK

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
Package 20190886215897
Primary 10190886215890

Customer Contacts

Device Sizes

Type Value Unit Text
Width .025 Inch
Height .014 Inch