Hartmann Cup Forceps 3mm/9cm 10-092-12

GUDID G25010092120

A long, thin, hand-held manual surgical instrument designed to facilitate grasping and manipulation of soft-tissues/anatomical structures [typically during ear/nose/throat (ENT) surgery]; it is not intended for insertion through an endoscope, nor into the eye, and is not a dedicated biopsy device. Commonly referred to as alligator- or crocodile-forceps, it has a slender body (to allow for restricted access) and small grasping blades which are hinged close to the distal (working) end. It is a metallic device available in various sizes/lengths; some types may include an integrated suction channel. This is a reusable device intended to be sterilized prior to use.

N S SURGICAL COMPANY

Surgical soft-tissue manipulation forceps, alligator, reusable
Primary Device IDG25010092120
NIH Device Record Keyf39314ac-e672-4594-8efc-a38810e2659e
Commercial Distribution StatusIn Commercial Distribution
Brand NameHartmann Cup Forceps 3mm/9cm
Version Model Number10-092-12
Catalog Number10-092-12
Company DUNS645681649
Company NameN S SURGICAL COMPANY
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Dimensions

Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
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Length9 Centimeter
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Length9 Centimeter
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Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0
Length9 Centimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCG25010092120 [Primary]

FDA Product Code

KAEForceps, Ent

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


[G25010092120]

Ultraviolet Light;Ethylene Oxide;Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-08
Device Publish Date2023-04-29

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