Medtlet 30-13-01

GUDID M9923013010

Medt Let I lancing device

Carelife (usa) Inc.

Manual blood lancing device, reusable
Primary Device IDM9923013010
NIH Device Record Keyab16c95f-8b84-4b19-b4b5-973842b0cd8b
Commercial Distribution StatusIn Commercial Distribution
Brand NameMedtlet
Version Model Number1
Catalog Number30-13-01
Company DUNS065756949
Company NameCarelife (usa) Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com
Phone7709356499
Emailli@carelifeusa.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM9923013010 [Primary]
HIBCCM9923013013 [Package]
Package: inner box [100 Units]
In Commercial Distribution
HIBCCM9923013015 [Package]
Contains: M9923013013
Package: corrugate carton [4 Units]
In Commercial Distribution

FDA Product Code

QRLMultiple Use Blood Lancet For Single Patient Use Only

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-08
Device Publish Date2023-10-31

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