Acu-Scissors

GUDID 00814105021101

Acu-Scissors, Straight, Sterile, 5/Bx

ACUDERM, INC.

General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use General-purpose surgical scissors, single-use

Primary Device ID	00814105021101
NIH Device Record Key	b54fd1ba-3002-42b9-934b-e8a7642e6153
Commercial Distribution Status	In Commercial Distribution
Brand Name	Acu-Scissors
Version Model Number	SCS
Company DUNS	071426803
Company Name	ACUDERM, INC.
Device Count	5
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	true
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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814105021101 [Unit of Use]
GS1	10814105021108 [Primary]

FDA Product Code

LRW	Scissors, General, Surgical

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2020-09-30
Device Publish Date	2020-09-22

On-Brand Devices [Acu-Scissors]

00814105021118	Acu-Scissors, Curved, Sterile, 5/Bx
00814105021101	Acu-Scissors, Straight, Sterile, 5/Bx