Home GUDID 00732094239140 Welch Allyn, Inc.
Primary DI 00732094239140
Brand Welch Allyn, Inc.
Company WELCH ALLYN, INC.
Model 901071
Catalog number 411251
Device description 590 LARGE DLV ASSEMBLY
Published 2017-12-05
Public version status Update
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name HIB Speculum, vaginal, nonmetal
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class HIB Speculum, Vaginal, Nonmetal Obstetrics/Gynecology 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 00732094236347 Package GS1 1 In Commercial Distribution 00732094236545 Package GS1 4 In Commercial Distribution 00732094239140 Package GS1 14 In Commercial Distribution 00732094239157 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 00732094236347 00732094236347 732094236347 0732094236347 00732094236545 00732094236545 732094236545 0732094236545 00732094239140 00732094239140 732094239140 0732094239140 00732094239157 00732094239157 732094239157 0732094239157
GMDN Terms# Term, Definition table Term Definition Vaginal speculum, single-use A hand-held manual instrument intended to dilate the vagina after insertion, typically for visual examination of the vaginal canal and cervix and/or to perform a gynaecological procedure. It typically consists of two long blades, joined at a handle at one end, that are inserted into the vagina in a horizontal position and then opened to form an angle, or it is a soft-material device inflated after insertion that allows viewing and access through a central channel. It is typically made entirely of plastic materials or has removable blades made of plastic. This is a single-use device.
Regulatory Flags# DUNS number 198227881 Device count 1 DM exempt false Premarket exempt false 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 00732094323931 Welch Allyn, Inc. 901139 S2-P-AXX-XXX 2023-08-25 00732094272222 Welch Allyn, Inc. 901145 33193-001-51 2019-09-26 00732094262551 Welch Allyn, Inc. 901011 SCNODE-DEB-CXXXX 2019-09-25 00732094288773 Welch Allyn, Inc. 901144 108191 2020-11-10 00732094288780 Welch Allyn, Inc. 901144 108190 2020-11-10 00732094272086 Welch Allyn, Inc. 901095 41000-032-57 2020-02-19 00732094272154 Welch Allyn, Inc. 901145 33193-106-53 2019-09-26 00732094272161 Welch Allyn, Inc. 901145 33193-106-52 2019-09-26 00732094272178 Welch Allyn, Inc. 901145 33193-106-51 2019-09-26 00732094271782 Welch Allyn, Inc. 901007 ACC-ELI280-A 2019-07-24 00732094265125 Welch Allyn, Inc. 901134 ESWK-AEB-BXXXX 2019-09-17 00732094271812 Welch Allyn, Inc. 901095 ACC-BUR280-B 2019-09-13 00732094272116 Welch Allyn, Inc. 901095 41000-031-57 2019-09-13 00732094271768 Welch Allyn, Inc. 901007 ACC-ELI380-A 2019-09-12 00732094322866 Welch Allyn, Inc. 901134 ESCRIBE-CAX-DXACB 2019-07-22 00732094322873 Welch Allyn, Inc. 901134 ESCRIBE-CAX-CXXXX 2019-07-22 00732094322880 Welch Allyn, Inc. 901134 ESCRIBE-CAX-CXACX 2019-07-22 00732094322897 Welch Allyn, Inc. 901134 ESCRIBE-CAX-CXACA 2019-07-22 00732094322903 Welch Allyn, Inc. 901134 ESCRIBE-BEX-CXXXA 2019-07-22 00732094322910 Welch Allyn, Inc. 901134 ESCRIBE-BEX-CXXCA 2019-07-22
Other Devices Sharing Product Codes# 
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