Air Mattress, Dial Operated Pump, Single Cell

GUDID 00616784044217

DYNAREX CORPORATION

Basic bed mattress Basic bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress Alternating-pressure bed mattress

Primary Device ID	00616784044217
NIH Device Record Key	51bf0a0c-f0d9-4509-91cb-cf4f3f1c2095
Commercial Distribution Status	In Commercial Distribution
Brand Name	Air Mattress, Dial Operated Pump, Single Cell
Version Model Number	10442
Company DUNS	008124539
Company Name	DYNAREX CORPORATION
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	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00616784044217 [Primary]

FDA Product Code

FNM	Mattress, Air Flotation, Alternating Pressure

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2018-06-25
Device Publish Date	2018-05-23

On-Brand Devices [Air Mattress, Dial Operated Pump, Single Cell]

00616784044227	10442
00616784044217	10442