AccessGUDID - DEVICE: Sentient Manufacturing (00860007603754)

GUDID

Device Identifier (DI) Information

Brand Name: Sentient Manufacturing
Version or Model: 3041340
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number:
Company Name: Sentient Manufacturing, LLC

Primary DI Number: 00860007603754
Issuing Agency: GS1
Commercial Distribution End Date: September 07, 2023
Device Count: 1
Labeler D-U-N-S® Number*: 106674754 *Terms of Use

Device Description: Sentient Manufacturing Laser Fiber Stripper

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	No
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
48018	Laser fibre stripper	A non-sterile, hand-held device used by authorized medical personnel to strip the outer protective layer (i.e., casing, jacket or buffer) from the end of a laser fibreoptic device without damaging the fibreoptics so that the bared end can be prepared for the next procedure (e.g, cleaving and repair). It is available in various designs and configurations, e.g., in the form of an electrical cable stripper (a pliers-like device) with two blades that hinge at a proximal end which are clamped over the fibreoptic device to be stripped and a mechanically adjustable depth limiter. It is configured to accept and strip one size or type of fibreoptic.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEX	Powered Laser Surgical Instrument

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: No
Requires Sterilization Prior to Use: Yes

Sterilization Method [?]
Moist Heat or Steam Sterilization

Storage and Handling

[?]

Storage and Handling
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: f199bd5b-cef3-474d-9366-2f9215ada33c
Public Version Date: October 18, 2023
Public Version Number: 2
DI Record Publish Date: September 16, 2022