FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 10705034479262 · Model: 698341662 · DEPUY SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
10705034479262
Version / Model
698341662
Catalog Number
698341662
Company Name
DEPUY SPINE, LLC
Labeler DUNS
107105876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-14
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
42d6e929-4ba9-4b1c-bf38-1e2d87b5ca41

Device Description

MODIFIED INSTRUMENT SUCTION COBB

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
GCX APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

GMDN Terms

Code Name
35048 Bone lever/elevator, reusable

Identifiers

Type ID
Primary 10705034479262

Customer Contacts