WIRE CRIMPING ALLIGATOR FORCEPS 4 MM X .8 MM JAW

GUDID 00821925012172

Gyrus Acmi, Inc.

Rigid endoscopic grasping forceps, reusable

Primary Device ID	00821925012172
NIH Device Record Key	c32a27d1-5a73-43ff-b5be-90bcc1b4c683
Commercial Distribution Status	In Commercial Distribution
Brand Name	WIRE CRIMPING ALLIGATOR FORCEPS 4 MM X .8 MM JAW
Version Model Number	131226
Company DUNS	007198742
Company Name	Gyrus Acmi, 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	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00821925012172 [Primary]

FDA Product Code

JXX	FORCEPS, WIRE CLOSURE, ENT, STERILE

Sterilization

Steralize Prior To Use	true
Device Is Sterile	false

[00821925012172]

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Moist Heat or Steam Sterilization

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Moist Heat or Steam Sterilization

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Moist Heat or Steam Sterilization

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Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

[00821925012172]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2018-10-11
Device Publish Date	2018-09-10

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