FDA UDI Not in Commercial Distribution 🇺🇸 United States

Sentient Manufacturing

DI: 00860007603754 · Model: 3041340 · Sentient Manufacturing, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Sentient Manufacturing
Primary DI
00860007603754
Version / Model
3041340
Company Name
Sentient Manufacturing, LLC
Labeler DUNS
106674754
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-09-16
Public Version
2
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
f199bd5b-cef3-474d-9366-2f9215ada33c
Distribution End Date
2023-09-07

Device Description

Sentient Manufacturing Laser Fiber Stripper

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
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
GEX Powered Laser Surgical Instrument

GMDN Terms

Code Name
48018 Laser fibre stripper

Identifiers

Type ID
Primary 00860007603754