Primary Device ID | 30886158002537 |
NIH Device Record Key | 86a74813-a472-4918-aee2-8c5d2b7df38b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Visitec® |
Version Model Number | 581610 |
Catalog Number | 581610 |
Company DUNS | 001406024 |
Company Name | Beaver-Visitec International, Inc. |
Device Count | 1 |
DM Exempt | false |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com | |
Phone | +1(866)906-8080 |
customersupport@bvimedical.com |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Special Storage Condition, Specify | Between 0 and 0 *Store in a dry place. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 30886158002537 [Primary] |
HNY | Cystotome |
Steralize Prior To Use | true |
Device Is Sterile | true |
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
[30886158002537]
Radiation Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-05 |
Device Publish Date | 2024-06-27 |
00886158021483 | Viscoflow® Cannula .30 x 22mm (30G x 7/8in) 10 |
00886158101420 | CYSTOTOME IRRIGATING STRGHT 27G 5/8IN (10/SP) |
00886158101413 | Irrigating Cystotome [Blumenthal] .40 x 16mm (27G x 5/8in) 10 |
00886158101406 | Bishop Harmon Cannula 1.1 x 25mm (19G x 1in) 10 |
00886158101390 | Irrigating Cystotome [Joyce] .40 x 16mm (26G x 5/8in) 10 |
00886158101383 | IOL Manipulator [Lester] .25mm 3 |
00886158101376 | CANN SUBRETINAL 20G CURVED (5/SP) |
00886158101369 | Irrigating Cystotome (Reverse) .50 x 16mm (25G x 5/8in) 10 |
00886158101352 | Lacrimal Cannula [Shahinian] .60 x 12mm (23G x 1/2in) 5 |
00886158101345 | Small Incision Irrigating Vectis [Pearce] .40mm (27G) 5 |
00886158101338 | Lacrimal Trephine [Sisler] .80mm x 38mm (21G x 1 1/2in 3 |
00886158101321 | Irrigating Cystotome [Joyce] .50 x 16mm (25G x 5/8in) 10 |
00886158101314 | Micro J Shape Hydrodissector [Pearce] .40 x 22mm (27G x 7/8in) 10 |
00886158101291 | Subretinal Fluid Cannula 6mm [Grizzard] .90mm (20G) 5 |
00886158101284 | Sharp Point Cystotome .70 x 27mm (22G x 1 1/16in) 5 |
00886158101277 | Retrobulbar (Curved) [Atkinson / Straus] .50 x 34mm (25G x 1 3/8in 10 |
00886158101260 | Lacrimal Cannula 1.1 x 20mm (19G x 3/4in) 5 |
00886158101253 | Nucleus Hydrodelineator [P. Koch] .50mm x 22mm (25G x 7/8in) 10 |
00886158101246 | Lacrimal Intubation with Retrieval Device .60mm x 11cm (23G x 4 1/4in) 3 |
00886158101239 | DCR Set (Angled) [O'Donoghue] .90mm x 4.5cm (20G x 1 3/4in) |
00886158101222 | DCR Set (Straight) [O'Donoghue] .90mm x 4.5cm (20G x 1 3/4in) 3 |
00886158101215 | Lacrimal Intubation .60mm x 17.5cm (23G x 7in) 3 |
00886158101208 | Irrigating Cystotome .40 x 16mm (27G x 5/8in) 10 |
00886158101192 | Irrigating Cystotome .50 x 16mm (25G x 5/8in) 10 |
00886158006534 | Flexible Tip Cannula .50 x 22mm (25G x 7/8in) 10 |
00886158006527 | Nucleus Hydrodissector [Pearce] .40 x 22mm (27G x 7/8in) 10 |
00886158006510 | Viscoflow® Cannula .30 x 22mm (30G x 7/8in) 10 P |
00886158006503 | Irrigating Cystotome [Blumenthal] .40 x 16mm (27G x 5/8in) 10 |
00886158006442 | Micro J Shape Cannula .40 x 22mm (27G x 7/8in) 10 |
00886158002796 | Flexible Tip Cannula .60 x 22mm (23G x 7/8in) 10 |
00886158002789 | Nucleus Hydrodissector [Pearce] .50 x 22mm (25G x 7/8in) 10 |
00886158002772 | Peribulbar [Atkinson] .50 x 22mm (25G x 7/8in) 10 |
00886158002765 | Viscoflow® Cannula .40 x 22mm (27G x 7/8in 10 |
00886158002758 | Anterior Chamber Cannula [Rycroft] .60 x 22mm (23G x 7/8in) 10 |
00886158002741 | Viscoflow® Cannula .60 x 22mm (23G x 7/8in 10 |
00886158002734 | Viscoflow® Cannula [Formed] .40 x 22mm (27G x 7/8in) 10 |
00886158002727 | Anterior Chamber Cannula .40 x 22mm (27G x 7/8in) 10 |
00886158002710 | Flexible Tip Cannula .40 x 22mm (27G x 7/8in 10 |
00886158002703 | Micro J Shape Cannula .50 x 22mm (25G x 7/8 in) 10 |
00886158002697 | Retrobulbar/Peribulbar [Atkinson] .60 x 32mm (23G x 1 1/4 in) 10 |
00886158101307 | IOL Manipulator [Jaffe / Maltzman] Blunt Tip (45 degree) 3 |
00886158101826 | Infusion Cannula 6mm .90mm (20G) |
00886158101802 | Blunt Tip Irrigating Cystotome [Kellan] .50 x 22mm (25G x 7/8in) |
00886158101796 | Vitreoretinal Micropick [Glaser] .50 x 5mm (25G x 3/16in) (50 Degrees) |
00886158101789 | Irrigating Cystotome [Blumenthal] .50 x 16mm (25G x 5/8in) |
00886158101765 | I and A Cannula [Simcoe] .60mm / .60mm (23G / 23G) |
30886158101759 | Tapered Hydrodelineator [Blumenthal] .50 x 22mm (25G x 7/8in) (45 degree) |
30886158101742 | Retrobulbar/Perbulbar [Atkinson] .50 x 32mm (25G x 1 1/4 in) |
30886158101735 | I and A Cannula [Dahan-Simcoe] .60mm / .60mm (23G / 23G) |
30886158101704 | Eye Speculum [Kratz / Barraquer] 40 x 26.5mm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VISITEC 73587740 1434606 Live/Registered |
VISITEC COMPANY 1986-03-13 |
VISITEC 73364521 1250239 Dead/Cancelled |
Visitec Company 1982-05-13 |