Primary Device ID | 10609271950150 |
NIH Device Record Key | b101e8ed-4578-41ba-a0f4-16fd1a7e4044 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MECRON Belt B: 29 cm, U: 84-110 cm |
Version Model Number | 38-7430 |
Catalog Number | 38-7430 |
Company DUNS | 184231298 |
Company Name | DARCO INTERNATIONAL, INC. |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 00609271950153 [Primary] |
GS1 | 10609271950150 [Package] Contains: 00609271950153 Package: Box [12 Units] In Commercial Distribution |
IPX | ORTHOSIS, RIB FRACTURE, SOFT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-22 |
Device Publish Date | 2023-02-14 |
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