FDA UDI Not in Commercial Distribution 🇺🇸 United States

GENERIC

DI: 00841732131811 · Model: 061.7555 · CTL Medical Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
GENERIC
Primary DI
00841732131811
Version / Model
061.7555
Company Name
CTL Medical Corporation
Labeler DUNS
080138504
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-21
Public Version
2
Public Version Date
2026-04-13
Public Version Status
Update
Public Device Record Key
f2d89bc1-e51a-4c67-8524-596a1fd30f8f
Distribution End Date
2026-04-10

Device Description

Additional Blade Connector

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
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
GFA Blade, Saw, General & Plastic Surgery, Surgical

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00841732131811

Customer Contacts