Feiman

GUDID 06976833926005

Zhejiang Feiman Medical Technology Co., Ltd.

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Primary Device ID	06976833926005
NIH Device Record Key	43ae32f3-062e-4cf5-a6eb-b2fefb6133b8
Commercial Distribution Status	In Commercial Distribution
Brand Name	Feiman
Version Model Number	AT600
Company DUNS	715058571
Company Name	Zhejiang Feiman Medical Technology Co., Ltd.
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	false
Serial Number	true
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06976833926005 [Primary]

FDA Product Code

GDC	Table, Operating-Room, Electrical

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	2023-12-08
Device Publish Date	2023-11-30