FDA UDI In Commercial Distribution 🇺🇸 United States

NexGen®

DI: 00889024201699 · Model: 00-5901-035-33 · Zimmer, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

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Basic Information

Brand Name
NexGen®
Primary DI
00889024201699
Version / Model
00-5901-035-33
Catalog Number
00-5901-035-33
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2016-10-28
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
94123f7c-9b49-46b7-8529-3884cd2f4fee

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
No
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 00889024201699
Unit of Use 00889024466418

Customer Contacts

Device Sizes

Type Value Unit Text
Length 33 Millimeter
Device Size Text, specify 3.5 mm Hex Head Screw, 3.2 mm, Diameter