FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 10705034581194 · Model: 698344937 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
N/A
Primary DI
10705034581194
Version / Model
698344937
Catalog Number
698344937
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-07-23
Public Version
1
Public Version Date
2024-07-31
Public Version Status
New
Public Device Record Key
dcfa80da-ec24-4228-abf1-4d7c85cf5531

Device Description

MODIFIED INSTRUMENT RETRACTOR,MEDIUM

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
No

Product Codes

Code Name
GAD RETRACTOR

GMDN Terms

Code Name
46774 Surgical retractor/retraction system blade, reusable

Identifiers

Type ID
Primary 10705034581194

Customer Contacts