Omni Life Sc.

GUDID B504OM414810020

Provision

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Primary Device ID	B504OM414810020
NIH Device Record Key	3af9a54d-a2c2-414c-a747-5d118329288c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Omni Life Sc.
Version Model Number	4148-1002
Company DUNS	016889401
Company Name	Provision
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	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	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504OM414810020 [Primary]

FDA Product Code

LXH	Orthopedic Manual Surgical Instrument

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	2024-05-27
Device Publish Date	2024-05-17

On-Brand Devices [Omni Life Sc.]

B504OM414810050	4148-1005
B504OM414810040	4148-1004
B504OM414810020	4148-1002
B504OM414810010	4148-1001
B504OM414550030	4145-5003