FDA UDI In Commercial Distribution 🇺🇸 United States

BOSS Instruments

DI: 00888515248939 · Model: 95-9120 · BOSS INSTRUMENTS, LTD., INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
BOSS Instruments
Primary DI
00888515248939
Version / Model
95-9120
Catalog Number
95-9120
Company Name
BOSS INSTRUMENTS, LTD., INC.
Labeler DUNS
848522678
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-27
Public Version
1
Public Version Date
2024-03-06
Public Version Status
New
Public Device Record Key
167787b3-85d3-44f1-9344-b4479dca50ea

Device Description

Handle for use with 95-9121 through 95-9134

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
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
KTG KNIFE, ENT

GMDN Terms

Code Name
38105 Laryngeal knife

Identifiers

Type ID
Primary 00888515248939

Customer Contacts