FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10886982131966 · Model: 09.037.010S · Synthes GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10886982131966
Version / Model
09.037.010S
Catalog Number
09037010S
Company Name
Synthes GmbH
Labeler DUNS
486711679
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-31
Public Version
5
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
b21141b3-a082-4dcb-a3ed-ac3dfe3cf408

Device Description

3.2MM GUIDE WIRE 475MM STERILE

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FZX Guide, surgical, instrument

GMDN Terms

Code Name
46165 Orthopaedic guidewire, reusable

Identifiers

Type ID
Secondary H67909037010S0
Primary 10886982131966

Customer Contacts