FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 20886982305968 · Model: SD02.111.500 · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
NA
Primary DI
20886982305968
Version / Model
SD02.111.500
Catalog Number
SD02111500
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-04-21
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
a901b867-cb77-4baa-8a63-c822637858e4

Device Description

1MM REDUCTION WIRE

Device Characteristics

Single Use
No
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Unit of Use 80886982305960
Primary 20886982305968

Customer Contacts