25GA Flexible 41GA Cannula

GUDID 10632307001533

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

Primary Device ID	10632307001533
NIH Device Record Key	2ea4b075-5929-471c-9fef-1ca691bb07a3
Commercial Distribution Status	In Commercial Distribution
Brand Name	25GA Flexible 41GA Cannula
Version Model Number	PD225.41
Company DUNS	622467348
Company Name	PEREGRINE SURGICAL, LTD.
Device Count	1
DM Exempt	true
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Customer Support Contacts

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

Device Dimensions

Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00632307001536 [Primary]
GS1	10632307001533 [Package] Contains: 00632307001536 Package: Box [5 Units] In Commercial Distribution

FDA Product Code

HMX	CANNULA, OPHTHALMIC

Sterilization

Steralize Prior To Use	true
Device Is Sterile	true

[10632307001533]

Ethylene Oxide

[10632307001533]

Ethylene Oxide

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	6
Public Version Date	2019-10-07
Device Publish Date	2016-05-06

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

10632307001533	25GA Flexible 41GA Cannula
10632307002318	25GA Flexible 41GA Cannula