Microsharp® 377531

GUDID 30886158001493

KNIFE 30 DEG 3.5MM DEPTH S/SU BLACK (10/SP)

Beaver-Visitec International, Inc.

Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use Ophthalmic knife, single-use
Primary Device ID30886158001493
NIH Device Record Key33b278d4-6855-40a9-9547-feb676d65ab2
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicrosharp®
Version Model Number377531
Catalog Number377531
Company DUNS001406024
Company NameBeaver-Visitec International, Inc.
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 Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com
Phone+1(866)906-8080
Emailcustomersupport@bvimedical.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a dry place.

Device Identifiers

Device Issuing AgencyDevice ID
GS130886158001493 [Primary]

FDA Product Code

HNNKnife, ophthalmic

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


[30886158001493]

Radiation Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-14
Device Publish Date2024-06-06

On-Brand Devices [Microsharp®]

30886158001516KNIFE 45 DEG 3.0MM DEPTH S/SU TAN (10/SP)
30886158001493KNIFE 30 DEG 3.5MM DEPTH S/SU BLACK (10/SP)
30886158001486BLADE 30 DEG 3.5MM DEPTH S/SU BLACK (6/SP)
30886158001479KNIFE 22.5 DEG 4MM DEPTH S/SU LIGHT BL (10/SP)
30886158001462BLADE 22.5 DEG 4MM DEPTH S/SU LIGHT BL (6/SP)
30886158001417KNIFE 15 DEG 1.5MM DEPTH S/SU ORN (10/SP)
30886158001400BLADE 15 DEG 1.5MM DEPTH S/SU ORN (6/SP)
30886158000809BLADE 15 DEG 5.0MM DEPTH S/S UGN (50/SP)

Trademark Results [Microsharp]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MICROSHARP
MICROSHARP
76010223 not registered Dead/Abandoned
Micro Sharp Inc.
2000-03-27
MICROSHARP
MICROSHARP
76010222 not registered Dead/Abandoned
Micro Sharp Inc.
2000-03-27
MICROSHARP
MICROSHARP
74576588 not registered Dead/Abandoned
Nashua Corporation
1994-09-21
MICROSHARP
MICROSHARP
73685554 1521571 Dead/Cancelled
REMINGTON PRODUCTS, INC.
1987-09-21
MICROSHARP
MICROSHARP
73560178 1437253 Dead/Cancelled
UCHIDA OF AMERICA, CORP.
1985-09-26
MICROSHARP
MICROSHARP
73504525 1335475 Dead/Cancelled
Pentech International Inc.
1984-10-18
MICROSHARP
MICROSHARP
72361886 0942190 Dead/Expired
SHANDON SCIENTIFIC COMPANY LIMITED
1970-06-05

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.