Primary Device ID | 06973175530266 |
NIH Device Record Key | e70c402a-0d3a-4005-9737-5c4e57b7d4c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | JBH |
Version Model Number | D26 |
Company DUNS | 554547530 |
Company Name | Anhui JBH Medical Apparatus Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 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 | 06973175530266 [Primary] |
ITI | Wheelchair, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-26 |
Device Publish Date | 2025-05-16 |
06973175532314 | D09 |
06973175530556 | DC03 |
06973175530402 | D25 |
06973175530426 | DC10L |
06973175530372 | D36 |
06973175530679 | D16 |
06973175530419 | DC07L |
06973175530280 | DC02 |
06973175530266 | D26 |
06973175530228 | DC03 |
06973175530204 | FDB01 |
06973175530181 | D15 |
06973175530167 | D12 |
06973175530150 | D11 |
06973175530112 | D09 |
06973175530075 | D05 |
06973175530044 | FDB02 |
06973175530006 | D10 |