20GA 1mm Bipolar Pick - Universal

GUDID 10632307001090

20GA 1mm Bipolar Pick - Universal

PEREGRINE SURGICAL, LTD.

Ophthalmic fibreoptic light instrument, single-use
Primary Device ID10632307001090
NIH Device Record Key8329c147-b388-4c87-a07c-973ddc08266a
Commercial Distribution StatusIn Commercial Distribution
Brand Name20GA 1mm Bipolar Pick - Universal
Version Model NumberPD100.15
Company DUNS622467348
Company NamePEREGRINE SURGICAL, LTD.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com
Phone+1(215)348-0456
Emailryan@peregrine-surgical.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0
Needle Gauge20 Gauge
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100632307001093 [Primary]
GS110632307001090 [Package]
Contains: 00632307001093
Package: Box [5 Units]
In Commercial Distribution

FDA Product Code

MPAEndoilluminator

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

[10632307001090]

Ethylene Oxide

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-07
Device Publish Date2016-05-06

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