FDA UDI In Commercial Distribution 🇺🇸 United States

Transom™

DI: 00841508103189 · Model: 11-90-009 · NEUROSTRUCTURES, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Transom™
Primary DI
00841508103189
Version / Model
11-90-009
Company Name
NEUROSTRUCTURES, INC
Labeler DUNS
079391677
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-06
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
102c2246-e183-4126-9266-932b2dd67c87

Device Description

All in One Variable Guide - Double Barrel

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
Yes
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 00841508103189

Customer Contacts

Phone
8003526103