MANI Sutures PGA 502

GUDID 04546951525507

Polyglycolic acid suture

Primary Device ID	04546951525507
NIH Device Record Key	49ec3539-96a1-43bb-a625-b3f4f1b93421
Commercial Distribution Status	In Commercial Distribution
Brand Name	MANI Sutures PGA
Version Model Number	502
Catalog Number	502
Company DUNS	690622428
Company Name	MANI, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	true
Serial Number	false
Manufacturing Date	true
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	04546951525507 [Primary]

GAM	Suture, Absorbable, Synthetic, Polyglycolic Acid

Steralize Prior To Use	false
Device Is Sterile	true