MT

GUDID 06975808860146

JIANGSU MJD MEDICAL TECHNOLOGY CO.,LTD.

Dermatome blade, reusable
Primary Device ID06975808860146
NIH Device Record Key5c711ae4-49f9-40c8-9c04-e9cdaa38b1a0
Commercial Distribution StatusIn Commercial Distribution
Brand NameMT
Version Model NumberMT-B-160
Company DUNS414588331
Company NameJIANGSU MJD MEDICAL TECHNOLOGY CO.,LTD.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106975808860146 [Primary]

FDA Product Code

GFDDermatome

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


[06975808860146]

Ethylene Oxide


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-22
Device Publish Date2025-01-14

On-Brand Devices [MT]

06975808860405MT-Q1
06975808860313MT-5
06975808860238MT-7C
06975808860214MT-7B
06975808860115MT-A-106
06975808860603MT-6
06975808861013MT-Q2
06975808861129MT-Q1B
06975808861235MT-Q3C
06975808861228MT-Q3B
06975808861211MT-Q3A
06975808860726MT-3c
06975808860719MT-3b
06975808860702MT-3a
06975808860146MT-B-160
06975808860139MT-B-80
06975808860122MT-A-160
06975808860108MT-A-80

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.