Home GUDID 00732094107951 Welch Allyn, Inc.
Primary DI 00732094107951
Brand Welch Allyn, Inc.
Company WELCH ALLYN, INC.
Model 901001
Catalog number 411510
Device description 4MM TIPS WITH SLEEVE
Published 2023-11-03
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name ERA OTOSCOPE
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class ERA Otoscope Ear, Nose, Throat 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00732094107951 Package GS1 20 In Commercial Distribution 00732094144260 Package GS1 10 In Commercial Distribution 00732094230475 Primary GS1 0 00732094141979 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 00732094107951 00732094107951 732094107951 0732094107951 00732094144260 00732094144260 732094144260 0732094144260 00732094230475 00732094230475 732094230475 0732094230475 00732094141979 00732094141979 732094141979 0732094141979
GMDN Terms# Term, Definition table Term Definition Otoscope, direct An electrically-powered, hand-held device designed for examination of the outer ear canal and tympanic membrane (eardrum) by direct viewing through the ear opening. It consists of a main unit (commonly referred to as the head) with a built-in light source intended to illuminate the interior of the ear canal with a detachable cone-shaped tube (speculum) inserted in the ear canal; it may facilitate the application of air pressure for pneumatic otoscopy. A dedicated power supply handpiece and/or an insufflation bulb may be included with the head.
Regulatory Flags# DUNS number 198227881 Device count 25 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 false Donation ID number false Contains natural rubber latex false 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 00817655023106 Welch Allyn, Inc. 901145 419734 2019-10-23 00732094356366 Welch Allyn, Inc. 901006 9293-046-57 2025-09-22 00732094356373 Welch Allyn, Inc. 901006 9293-046-55 2025-09-22 00732094319903 Welch Allyn, Inc. 901011 419832 2023-09-26 00732094326079 Welch Allyn, Inc. 901006 9293-024-51 2023-08-25 00732094247138 Welch Allyn, Inc. 901031 39500-TE 2019-08-28 00732094247145 Welch Allyn, Inc. 901031 39500-NP-TE 2019-08-28 00732094272338 Welch Allyn, Inc. 901152 11094-001-50 2020-03-24 00732094258905 Welch Allyn, Inc. 901134 11012-014-50 2020-03-20 00732094307351 Welch Allyn, Inc. 901145 419751 2019-10-23 00732094307368 Welch Allyn, Inc. 901145 413379 2019-10-23 00732094307375 Welch Allyn, Inc. 901145 419733 2019-10-23 00732094258998 Welch Allyn, Inc. 901011 036840-005 2019-09-26 00732094272673 Welch Allyn, Inc. 901011 036840-006 2019-09-26 00817655020679 Welch Allyn, Inc. 901134 11012-016-50 2019-09-26 00817655020686 Welch Allyn, Inc. 901134 11012-016-51 2019-09-26 00732094296341 Welch Allyn, Inc. 901012 11093-003-50 2019-06-11 00732094223910 Welch Allyn, Inc. 901108 411215 2023-08-24 00732094089226 Welch Allyn, Inc. 901020 11840 2016-09-17 00732094089240 Welch Allyn, Inc. 901022 11820 2016-09-17
Other Devices Sharing Product Codes# 
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