MAI

GUDID 20809160295141

General surgical procedure kit, non-medicated, single-use

Primary Device ID	20809160295141
NIH Device Record Key	8919af7c-ca40-4027-86a0-9f53fb8fb751
Commercial Distribution Status	In Commercial Distribution
Brand Name	MAI
Version Model Number	81446
Company DUNS	092364462
Company Name	MEDICAL ACTION INDUSTRIES INC.
Device Count	1
DM Exempt	true
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	true
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Special Storage Condition, Specify	Between 0 and 0 *STORE AT ROOM TEMPERATURE
Special Storage Condition, Specify	Between 0 and 0
Special Storage Condition, Specify	Between 0 and 0 *STORE AT ROOM TEMPERATURE
Special Storage Condition, Specify	Between 0 and 0
Special Storage Condition, Specify	Between 0 and 0 *STORE AT ROOM TEMPERATURE
Special Storage Condition, Specify	Between 0 and 0

Device Issuing Agency	Device ID
GS1	10809160295144 [Primary]
GS1	20809160295141 [Package] Contains: 10809160295144 Package: [10 Units] In Commercial Distribution

FTN	Plastic surgery and accessories kit

Steralize Prior To Use	false
Device Is Sterile	true