Visitec® 585013

GUDID 00886158101246

Lacrimal Intubation with Retrieval Device .60mm x 11cm (23G x 4 1/4in) 3

Beaver-Visitec International, Inc.

Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher Lacrimal tube insertion hook/pusher
Primary Device ID00886158101246
NIH Device Record Keyd1d85fe5-a111-4af3-a1b5-e9728cb2900c
Commercial Distribution StatusIn Commercial Distribution
Brand NameVisitec®
Version Model Number585013
Catalog Number585013
Company DUNS001406024
Company NameBeaver-Visitec International, Inc.
Device Count3
DM Exemptfalse
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100886158101246 [Unit of Use]
GS130886158101247 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HNLProbe, Lachrymal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-09
Device Publish Date2021-11-01

On-Brand Devices [Visitec®]

00886158021483Viscoflow® Cannula .30 x 22mm (30G x 7/8in) 10
00886158101420CYSTOTOME IRRIGATING STRGHT 27G 5/8IN (10/SP)
00886158101413Irrigating Cystotome [Blumenthal] .40 x 16mm (27G x 5/8in) 10
00886158101406Bishop Harmon Cannula 1.1 x 25mm (19G x 1in) 10
00886158101390Irrigating Cystotome [Joyce] .40 x 16mm (26G x 5/8in) 10
00886158101383IOL Manipulator [Lester] .25mm 3
00886158101376CANN SUBRETINAL 20G CURVED (5/SP)
00886158101369Irrigating Cystotome (Reverse) .50 x 16mm (25G x 5/8in) 10
00886158101352Lacrimal Cannula [Shahinian] .60 x 12mm (23G x 1/2in) 5
00886158101345Small Incision Irrigating Vectis [Pearce] .40mm (27G) 5
00886158101338Lacrimal Trephine [Sisler] .80mm x 38mm (21G x 1 1/2in 3
00886158101321Irrigating Cystotome [Joyce] .50 x 16mm (25G x 5/8in) 10
00886158101314Micro J Shape Hydrodissector [Pearce] .40 x 22mm (27G x 7/8in) 10
00886158101291Subretinal Fluid Cannula 6mm [Grizzard] .90mm (20G) 5
00886158101284Sharp Point Cystotome .70 x 27mm (22G x 1 1/16in) 5
00886158101277Retrobulbar (Curved) [Atkinson / Straus] .50 x 34mm (25G x 1 3/8in 10
00886158101260Lacrimal Cannula 1.1 x 20mm (19G x 3/4in) 5
00886158101253Nucleus Hydrodelineator [P. Koch] .50mm x 22mm (25G x 7/8in) 10
00886158101246Lacrimal Intubation with Retrieval Device .60mm x 11cm (23G x 4 1/4in) 3
00886158101239DCR Set (Angled) [O'Donoghue] .90mm x 4.5cm (20G x 1 3/4in)
00886158101222DCR Set (Straight) [O'Donoghue] .90mm x 4.5cm (20G x 1 3/4in) 3
00886158101215Lacrimal Intubation .60mm x 17.5cm (23G x 7in) 3
00886158101208Irrigating Cystotome .40 x 16mm (27G x 5/8in) 10
00886158101192Irrigating Cystotome .50 x 16mm (25G x 5/8in) 10
00886158006534Flexible Tip Cannula .50 x 22mm (25G x 7/8in) 10
00886158006527Nucleus Hydrodissector [Pearce] .40 x 22mm (27G x 7/8in) 10
00886158006510Viscoflow® Cannula .30 x 22mm (30G x 7/8in) 10 P
00886158006503Irrigating Cystotome [Blumenthal] .40 x 16mm (27G x 5/8in) 10
00886158006442Micro J Shape Cannula .40 x 22mm (27G x 7/8in) 10
00886158002796Flexible Tip Cannula .60 x 22mm (23G x 7/8in) 10
00886158002789Nucleus Hydrodissector [Pearce] .50 x 22mm (25G x 7/8in) 10
00886158002772Peribulbar [Atkinson] .50 x 22mm (25G x 7/8in) 10
00886158002765Viscoflow® Cannula .40 x 22mm (27G x 7/8in 10
00886158002758Anterior Chamber Cannula [Rycroft] .60 x 22mm (23G x 7/8in) 10
00886158002741Viscoflow® Cannula .60 x 22mm (23G x 7/8in 10
00886158002734Viscoflow® Cannula [Formed] .40 x 22mm (27G x 7/8in) 10
00886158002727Anterior Chamber Cannula .40 x 22mm (27G x 7/8in) 10
00886158002710Flexible Tip Cannula .40 x 22mm (27G x 7/8in 10
00886158002703Micro J Shape Cannula .50 x 22mm (25G x 7/8 in) 10
00886158002697Retrobulbar/Peribulbar [Atkinson] .60 x 32mm (23G x 1 1/4 in) 10
00886158101307IOL Manipulator [Jaffe / Maltzman] Blunt Tip (45 degree) 3
00886158101826Infusion Cannula 6mm .90mm (20G)
00886158101802Blunt Tip Irrigating Cystotome [Kellan] .50 x 22mm (25G x 7/8in)
00886158101796Vitreoretinal Micropick [Glaser] .50 x 5mm (25G x 3/16in) (50 Degrees)
00886158101789Irrigating Cystotome [Blumenthal] .50 x 16mm (25G x 5/8in)
00886158101765I and A Cannula [Simcoe] .60mm / .60mm (23G / 23G)
30886158101759Tapered Hydrodelineator [Blumenthal] .50 x 22mm (25G x 7/8in) (45 degree)
30886158101742Retrobulbar/Perbulbar [Atkinson] .50 x 32mm (25G x 1 1/4 in)
30886158101735I and A Cannula [Dahan-Simcoe] .60mm / .60mm (23G / 23G)
30886158101704Eye Speculum [Kratz / Barraquer] 40 x 26.5mm

Trademark Results [Visitec]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VISITEC
VISITEC
73587740 1434606 Live/Registered
VISITEC COMPANY
1986-03-13
VISITEC
VISITEC
73364521 1250239 Dead/Cancelled
Visitec Company
1982-05-13

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