FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 10705034577814 · Model: 698345000 · 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
10705034577814
Version / Model
698345000
Catalog Number
698345000
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-02-05
Public Version
1
Public Version Date
2025-02-13
Public Version Status
New
Public Device Record Key
123f1687-01a8-49ef-9099-70f5d752b702

Device Description

MODIFIED INSTRUMENT REDUCTION SLEEVE

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
HWR DRIVER, PROSTHESIS

GMDN Terms

Code Name
37148 Laparoscopic access cannula, reusable

Identifiers

Type ID
Primary 10705034577814

Customer Contacts