MED pro Medical B.V.

GUDID 08718455508270

Meatal Dilator 6/16

MED pro Medical B.V.

Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use Urethral dilator, single-use
Primary Device ID08718455508270
NIH Device Record Key1f173819-bbd8-4370-a902-ed3105ea2fe3
Commercial Distribution StatusIn Commercial Distribution
Brand NameMED pro Medical B.V.
Version Model NumberMD6/16
Company DUNS490059139
Company NameMED pro Medical B.V.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS108718455508270 [Primary]

FDA Product Code

KOEDilator, Urethral

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-19
Device Publish Date2022-09-09

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