FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00885556915288 · Model: 74038876 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
00885556915288
Version / Model
74038876
Catalog Number
74038876
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-17
Public Version
1
Public Version Date
2024-12-25
Public Version Status
New
Public Device Record Key
2efe7bca-d96a-4e6b-8dea-27b075b9819a

Device Description

LM/RL TIBIA ALIGNMENT GUIDE SHORT

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
LXH Orthopedic manual surgical instrument

GMDN Terms

Code Name
47870 Orthopaedic fixation implant alignment tool

Identifiers

Type ID
Primary 00885556915288

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify SHORT: SHORT

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
: -