Home GUDID 00810102271082 Dermapac, Inc.
Primary DI 00810102271082
Brand Dermapac, Inc.
Company Dermapac Inc.
Model 8034
Device description #32 Rubber Bands 5/pk
Published 2022-09-12
Public version status New
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 KDC Instrument, Surgical, Disposable
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KDC Instrument, Surgical, Disposable General, Plastic Surgery 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10810102271089 Primary GS1 0 00810102271082 Unit of Use GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, UPC-A table Source identifier GTIN-14 normalized UPC-A EAN-13 10810102271089 10810102271089 00810102271082 00810102271082 810102271082 0810102271082
GMDN Terms# Term, Definition table Term Definition General surgical procedure kit, non-medicated, single-use A typically non-dedicated collection of various surgical instruments, sometimes with dressings and/or other materials, but that does not contain pharmaceuticals, intended to be used during: 1) open abdominal surgery; 2) a range of open surgical procedures across multiple clinical specialties (non-dedicated); 3) non-orthopaedic trauma surgery; 4) minor dermatological surgery; or 5) cosmetic surgery below the head. As a kit that includes procedural devices, it is neither dedicated to surgical scrubbing, surgical patient preparation, nor anaesthesia, and is not a dedicated biopsy kit. This is a single-use device.
Regulatory Flags# DUNS number 796088466 Device count 50 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch false Serial number false Manufacturing date on label false Expiration date on label false Donation ID number false Contains natural rubber latex true No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 00810102270009 Dermapac, Inc. 1803 2022-09-12 00810102270016 Dermapac, Inc. 1804 2022-09-12 00810102270023 Dermapac, Inc. 1805 2022-09-12 00810102270030 Dermapac, Inc. 1809 2022-09-12 00810102270047 Dermapac, Inc. 1810 2022-09-12 00810102270054 Dermapac, Inc. 1812 2022-09-12 00810102270061 Dermapac, Inc. 1814 2022-09-12 00810102270078 Dermapac, Inc. 1815 2022-09-12 00810102270085 Dermapac, Inc. 1832 2022-09-12 00810102270092 Dermapac, Inc. 1860 2022-09-12 00810102270108 Dermapac, Inc. 2034 2022-09-12 00810102270115 Dermapac, Inc. 2036 2022-09-12 00810102270122 Dermapac, Inc. 2038 2022-09-12 00810102270139 Dermapac, Inc. 2080-B 2022-09-12 00810102270146 Dermapac, Inc. 2081 2022-09-12 00810102270153 Dermapac, Inc. 2087 2022-09-12 00810102270160 Dermapac, Inc. 2139 2022-09-12 00810102270177 Dermapac, Inc. 2140 2022-09-12 00810102270184 Dermapac, Inc. 2142 2022-09-12 00810102270191 Dermapac, Inc. 5003 2022-09-12
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