FDA UDI In Commercial Distribution 🇺🇸 United States

NEXUS

DI: 00192629410091 · Model: NEXTNSGD · Microport Orthopedics Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
NEXUS
Primary DI
00192629410091
Version / Model
NEXTNSGD
Catalog Number
NEXTNSGD
Company Name
Microport Orthopedics Inc.
Labeler DUNS
079118736
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-14
Public Version
1
Public Version Date
2025-07-22
Public Version Status
New
Public Device Record Key
bcb4bba0-a3b8-4147-9ad7-368fafb3f884

Device Description

NEXUS TRIAL NECK STD SZ 6-7

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
No
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
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Secondary M684NEXTNSGD1
Primary 00192629410091

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K250444 000