FDA UDI In Commercial Distribution 🇺🇸 United States

NEOORTHO

DI: 07899893220137 · Model: 908.143 · Neoortho Produtos Ortopédicos S/A.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NEOORTHO
Primary DI
07899893220137
Version / Model
908.143
Catalog Number
908.143
Company Name
Neoortho Produtos Ortopédicos S/A.
Labeler DUNS
914644351
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-05-16
Public Version
1
Public Version Date
2024-05-24
Public Version Status
New
Public Device Record Key
af508d25-12be-4476-a13b-581edb49f98b

Device Description

T15 Wrench

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary 07899893220137

Customer Contacts