Primary Device ID | 07506561200017 |
NIH Device Record Key | f4a8f0f3-ad86-434d-9bb5-6a6a7ec0c733 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INDALJIMTM |
Version Model Number | BS25-L |
Company DUNS | 812753058 |
Company Name | Indaljim, S.A. de C.V. |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07506561200017 [Primary] |
OEA | Non-Surgical Isolation Gown |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-07 |
Device Publish Date | 2022-01-28 |
07506561200277 | BE-01 |
07506561200260 | OV-XL |
07506561200253 | OV-L |
07506561200246 | OV-M |
07506561200239 | BMD-XL |
07506561200222 | BMD-L |
07506561200215 | BMD-M |
07506561200130 | C3C-01 |
07506561200062 | GR-01 |
07506561200055 | BS35-XL |
07506561200048 | BS35-L |
07506561200031 | BS35-M |
07506561200024 | BS25-XL |
07506561200017 | BS25-L |
07506561200000 | BS25-M |