FDA UDI Not in Commercial Distribution 🇺🇸 United States

Tube Biopsy Ui

DI: 04056481005092 · Model: 55970 · Brainlab AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tube Biopsy Ui
Primary DI
04056481005092
Version / Model
55970
Catalog Number
55970
Company Name
Brainlab AG
Labeler DUNS
314482980
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-15
Public Version
6
Public Version Date
2023-01-31
Public Version Status
Update
Public Device Record Key
c26ced2b-3453-4bb2-b3d3-6559b0bcfb93
Distribution End Date
2022-12-20

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
HAW Neurological Stereotaxic Instrument

GMDN Terms

Code Name
38723 Robotic surgical navigation system

Identifiers

Type ID
Primary 04056481005092

Customer Contacts

Phone
+49899915680

Premarket Submissions

Submission Number Supplement Number
K092467 000
K192703 000