RemoHip

GUDID 06973877662852

Ba Knife

Hangzhou Rejoin Mastin Medical Device Co., Ltd.

Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable Arthroscopic surgical procedure kit, non-medicated, reusable

Primary Device ID	06973877662852
NIH Device Record Key	2651653e-9ff3-480d-81fd-41c40c28bf23
Commercial Distribution Status	In Commercial Distribution
Brand Name	RemoHip
Version Model Number	801942400
Company DUNS	560430218
Company Name	Hangzhou Rejoin Mastin Medical Device 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	true
Serial Number	true
Manufacturing Date	true
Expiration Date	true
Donation Id Number	true
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	06973877662852 [Primary]

FDA Product Code

HWL	Set, Hollow Mill