Home GUDID 30748426073420 MICROTEK
Primary DI 30748426073420
Brand MICROTEK
Company MICROTEK MEDICAL, INC.
Model 1
Device description VIDEO CAMERA DRAPE
Published 2016-11-04
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name KKX Drape, surgical PUI Drape, surgical, exempt
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KKX Drape, Surgical General, Plastic Surgery 2 PUI Drape, Surgical, Exempt General, Plastic Surgery 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 30748426073420 Package GS1 25 In Commercial Distribution 50748426073424 Package GS1 1 In Commercial Distribution 00748426073429 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 30748426073420 30748426073420 50748426073424 50748426073424 00748426073429 00748426073429 748426073429 0748426073429
GMDN Terms# Term, Definition table Term Definition Medical equipment drape, single-use A flexible polymer sheet/bag/sleeve designed to form a protective water-resistant enclosure around a piece of medical equipment (e.g., C-arm, surgical laser/camera/microscope, examination table/chair) and/or equipment components (e.g., cables, tubes, headrest). It is intended as a hygienic barrier to protect the contents from soiling and contamination when used in the vicinity of, or entered into, a hygienic area. It is neither a dedicated handle cover, device cap nor an ultrasound transducer cover. This is a single-use device.
Storage And Handling# Type, Low, High table Type Low High Condition Special Storage Condition, Specify 0 0 Store under normal warehouse conditions.
Sterilization Methods# Method table Method Ethylene Oxide
Regulatory Flags# DUNS number 078516490 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label false Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00748426073429 MICROTEK 1 2016-11-04
Other Devices Sharing Product Codes# 
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