AccessGUDID - DEVICE: MicroFrance® (10381780094210)

GUDID

Device Identifier (DI) Information

Brand Name: MicroFrance®
Version or Model: CEV605GP
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: CEV605GP
Company Name: INTEGRA MICROFRANCE

Primary DI Number: 10381780094210
Issuing Agency: GS1
Commercial Distribution End Date: December 31, 2022
Device Count: 3
Labeler D-U-N-S® Number*: 276593071 *Terms of Use

Device Description: MicroFrance® Curved scissors insert, blades 15 mm, tube CEV8649GP CEV649GP CEV9649GP and sheath CEV8649C5 CEV649C5 CEV9649C5

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):	Yes
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?
33596	Endoscopic electrosurgical handpiece/electrode, monopolar, reusable	An electrosurgical device which consists of a handpiece with mechanical and/or electrical controls, and a monopolar electrode, intended to deliver electrosurgical current from a system generator directly to tissues for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery. It includes a long thin electrode connected to the handpiece, and may include a lumen for suction/irrigation; it is available in a variety of forms (e.g., forceps or snare with ring handles, rigid probe with controls) and requires a patient contact return electrode to complete the circuit. This is a reusable device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
GEI	ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

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
Special Storage Condition, Specify: No

Clinically Relevant Size

[?]

Size Type Text
No Device Sizes

Device Record Status

Public Device Record Key: 8f146efb-2800-407f-9a43-5fa4383c6653
Public Version Date: July 17, 2024
Public Version Number: 8
DI Record Publish Date: October 04, 2016