Tubing, with filter, sterile, for insuflation ONG04199ST119

GUDID 03700512905080

Promepla

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Primary Device ID	03700512905080
NIH Device Record Key	f98403ba-1eba-495b-901f-0a41df03c1e2
Commercial Distribution Status	In Commercial Distribution
Brand Name	Tubing, with filter, sterile, for insuflation
Version Model Number	WA95005A
Catalog Number	ONG04199ST119
Company DUNS	401020409
Company Name	Promepla
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	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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700512905080 [Primary]
GS1	14042761072639 [Package] Package: Box [20 Units] In Commercial Distribution

FDA Product Code

NKC	Tubing/Tubing With Filter, Insufflation, Laparoscopic

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	5
Public Version Date	2020-07-07
Device Publish Date	2016-09-23

On-Brand Devices [Tubing, with filter, sterile, for insuflation]

04042761072632	WA95005A
03700512905080	WA95005A