FDA UDI Not in Commercial Distribution 🇺🇸 United States

Accu-Beam

DI: B177911102022 · Model: 9111-0202 · TRANSAMERICAN TECHNOLOGIES INTERNATIONAL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Accu-Beam
Primary DI
B177911102022
Version / Model
9111-0202
Company Name
TRANSAMERICAN TECHNOLOGIES INTERNATIONAL
Labeler DUNS
130213366
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-05-26
Public Version
7
Public Version Date
2023-06-02
Public Version Status
Update
Public Device Record Key
248fe5f0-d75f-4d65-a01c-444c0adaf109
Distribution End Date
2022-06-29

Device Description

Rear cap for 14ga fiberoptic handpiece. Pack of 10.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
61474 General/multiple surgical laser system beam guide, reusable

Identifiers

Type ID
Primary B177911102022
Unit of Use B1779111020200

Premarket Submissions

Submission Number Supplement Number
K952006 000