BCG Vaccine (Multiple Puncture Device)

GUDID 60300858999993

MERCK SHARP & DOHME CORP.

Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet Allergy testing lancet
Primary Device ID60300858999993
NIH Device Record Keyd3018e01-0d77-45ff-a104-62f9f212d6e9
Commercial Distribution StatusIn Commercial Distribution
Brand NameBCG Vaccine (Multiple Puncture Device)
Version Model Number1039922
Company DUNS101740835
Company NameMERCK SHARP & DOHME CORP.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Producttrue
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com
Phone+1(404)218-5360
Emailsamuel.egas@merck.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100300858999991 [Primary]
GS160300858999993 [Package]
Contains: 00300858999991
Package: box [1 Units]
In Commercial Distribution

FDA Product Code

LDHSYSTEM, DELIVERY, ALLERGEN AND VACCINE

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


[60300858999993]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-18
Device Publish Date2023-04-10

Devices Manufactured by MERCK SHARP & DOHME CORP.

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60300520316813 - FOLLISTIM AQ Cartridge 600IU SAMPLE2019-11-05

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