FDA UDI In Commercial Distribution 🇺🇸 United States

IMACTIS®

DI: B681A102001 · Model: A10200 · IMACTIS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
IMACTIS®
Primary DI
B681A102001
Version / Model
A10200
Company Name
IMACTIS
Labeler DUNS
260527568
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-07
Public Version
3
Public Version Date
2025-09-23
Public Version Status
Update
Public Device Record Key
876f83df-f171-4f96-afd6-46e180b92f92

Device Description

Non-sterile needle holder of the IMACTIS® CT-NAVIGATION system

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
MR Unsafe
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
No

Product Codes

Code Name
JAK System, X-Ray, Tomography, Computed

GMDN Terms

Code Name
58183 Electromagnetic surgical navigation device tracking system

Identifiers

Type ID
Primary B681A102001

Premarket Submissions

Submission Number Supplement Number
K162314 000