BX Series Multi-Sampling Reusable Biopsy Forceps BX910N

GUDID M453BX910N0

Reusable biopsy forceps with serrated side fenestrated jaws capable of multiple sampling. HIBC/UPN: M453BX910N0

Primed Instruments Inc

Flexible endoscopic biopsy forceps, reusable
Primary Device IDM453BX910N0
NIH Device Record Key8944d601-6fe2-4d16-9b5e-99bac10d0bad
Commercial Distribution StatusIn Commercial Distribution
Brand NameBX Series Multi-Sampling Reusable Biopsy Forceps
Version Model NumberBX910N
Catalog NumberBX910N
Company DUNS254491293
Company NamePrimed Instruments 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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com
Phone1-877-565-0565
Emailinfo@primedendo.com

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Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.
Special Storage Condition, SpecifyBetween 0 and 0 *Biopsy forceps should be stored in the sterile package at room temperature in a clean and dry area away from direct sunlight. Each device is individually packaged.

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM453BX910N0 [Primary]

FDA Product Code

NONForceps, Biopsy, Non-Electric, Reprocessed

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


[M453BX910N0]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-03-08
Device Publish Date2021-02-26

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