Primary Device ID | 08806387814993 |
NIH Device Record Key | d0d5ce38-dc05-464c-bbe5-c5e9089681ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MG 02-15/40 LM |
Version Model Number | 1499 |
Company DUNS | 688322841 |
Company Name | Meta Biomed 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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 08806387814993 [Primary] |
EKM | Gutta-Percha |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-09-03 |
Device Publish Date | 2025-08-26 |
08806387814603 - MX 02-15 | 2025-09-03 MGP, 02 Taper 15, 60 Points, P.71 |
08806387814610 - MX 02-20 | 2025-09-03 MGP, 02 Taper 20, 60 Points, P.71 |
08806387814627 - MX 02-25 | 2025-09-03 MGP, 02 Taper 25, 60 Points, P.71 |
08806387814634 - MX 02-30 | 2025-09-03 MGP, 02 Taper 30, 60 Points, P.71 |
08806387814641 - MX 02-35 | 2025-09-03 MGP, 02 Taper 35, 60 Points, P.71 |
08806387814658 - MX 02-40 | 2025-09-03 MGP, 02 Taper 40, 60 Points, P.71 |
08806387814665 - MX 04-15 | 2025-09-03 MGP, 04 Taper 15, 60 Points, P.71 |
08806387814672 - MX 04-20 | 2025-09-03 MGP, 04 Taper 20, 60 Points, P.71 |