INFANT WIRE SPECULUM AE-1015

GUDID 00841668126516

INFANT WIRE SPECULUM

KATENA PRODUCTS, INC.

Eyelid speculum, reusable
Primary Device ID00841668126516
NIH Device Record Key418aa8ef-b43e-45f9-a76f-28bc4e776901
Commercial Distribution StatusIn Commercial Distribution
Brand NameINFANT WIRE SPECULUM
Version Model NumberAE-1015
Catalog NumberAE-1015
Company DUNS085668598
Company NameKATENA PRODUCTS, INC.
Device Count1
DM Exempttrue
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(973)989-1600
Emailinquiries.corzaeye@corza.com
Phone+1(973)989-1600
Emailinquiries.corzaeye@corza.com
Phone+1(973)989-1600
Emailinquiries.corzaeye@corza.com
Phone+1(973)989-1600
Emailinquiries.corzaeye@corza.com

Device Dimensions

Length4 Millimeter
Length4 Millimeter
Length4 Millimeter
Length4 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100841668126516 [Primary]

FDA Product Code

HNCSpecula, ophthalmic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-12-15
Device Publish Date2022-12-07

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