DMEK/DSAEK Forceps

GUDID 00632307002212

DMEK/DSAEK Forceps

PEREGRINE SURGICAL, LTD.

Ophthalmic soft-tissue manipulation forceps, probe-like, reusable
Primary Device ID00632307002212
NIH Device Record Key167a2fdd-74a9-4166-8229-50a1dc17ce11
Commercial Distribution Discontinuation2018-05-15
Commercial Distribution StatusNot in Commercial Distribution
Brand NameDMEK/DSAEK Forceps
Version Model NumberPD427.00
Company DUNS622467348
Company NamePEREGRINE SURGICAL, LTD.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com
Phone215-348-0456
Emailjayne@peregrine-surgical.com

Device Dimensions

Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge
Needle Gauge27 Gauge

Device Identifiers

Device Issuing AgencyDevice ID
GS100632307002212 [Primary]

FDA Product Code

HNRForceps, Ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


[00632307002212]

Moist Heat or Steam Sterilization;Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-07-12
Device Publish Date2018-03-23

On-Brand Devices [DMEK/DSAEK Forceps]

00632307002250DMEK/DSAEK Forceps
00632307002212DMEK/DSAEK Forceps

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