25GA Flexible 41GA Cannula

GUDID 10632307002318

25GA Flexible 41GA Cannula

PEREGRINE SURGICAL, LTD.

Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, single-use
Primary Device ID10632307002318
NIH Device Record Key4d8960ae-f371-4077-8f5d-3285ce2a885d
Commercial Distribution StatusIn Commercial Distribution
Brand Name25GA Flexible 41GA Cannula
Version Model Number1270.05-00
Company DUNS622467348
Company NamePEREGRINE SURGICAL, LTD.
Device Count1
DM Exempttrue
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 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
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

Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0
Needle Gauge25 Gauge
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100632307002311 [Primary]
GS110632307002318 [Package]
Contains: 00632307002311
Package: Box [5 Units]
In Commercial Distribution

FDA Product Code

HMXCANNULA, OPHTHALMIC

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

[10632307002318]

Ethylene Oxide

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-18
Device Publish Date2023-05-10

On-Brand Devices [25GA Flexible 41GA Cannula]

1063230700153325GA Flexible 41GA Cannula
1063230700231825GA Flexible 41GA Cannula
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