Primary Device ID | B33810K20301 |
NIH Device Record Key | 52e07fb6-3580-471e-a4ae-623d365fcc2f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EACU, EAKU, JOCU, ZAGU |
Version Model Number | 10K2030 |
Company DUNS | 421257620 |
Company Name | Maanshan Bond Medical Instruments Co., Ltd. |
Device Count | 1000 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 |
---|---|
HIBCC | B33810K20300 [Unit of Use] |
HIBCC | B33810K20301 [Primary] |
HIBCC | B33810K20302 [Package] Package: bigger box [10 Units] In Commercial Distribution |
MQX | Needle, Acupuncture, Single Use |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-18 |
Device Publish Date | 2016-09-22 |
B338PTN22162 | PTN2216 |
B338NKJ30752 | NKJ3075 |
B338NKJ25752 | NKJ2575 |
B338NKJ25152 | NKJ2515 |
B338NKJ16301 | NKJ1630 |
NKJ14302 | NKJ1430 |
B338IDN12052 | IDN1205 |
B338HB18081 | HB1808 |
B338DPB20072 | DPB2007 |
B338DPB18072 | DPB1807 |
B338DPB16071 | DPB1607 |
B338CB35251 | CB3525 |
B33810K22301 | 10K2230 |
B33810K22151 | 10K2215 |
B33810K20301 | 10K2030 |
B33810K20151 | 10K2015 |
B33810K18402 | 10K1840 |
B33810K18301 | 10K1830 |
B33810K18151 | 10K1815 |
B33810K16301 | 10K1630 |
B3385NKJ25402 | 5NKJ2540 |
B3385NKJ25302 | 5NKJ2530 |
B3385NKJ22402 | 5NKJ2240 |
B3385NKJ22302 | 5NKJ2230 |
B3385NKJ20302 | 5NKJ2030 |
B3385NKJ18300 | 5NKJ1830 |
B3385NKJ16400 | 5NKJ1640 |
B3385NKJ16300 | 5NKJ1630 |