Primary Device ID | 00857878007057 |
NIH Device Record Key | 7cb992b8-7b9a-4c9c-81d0-eb668ef6f3b5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 18-40-0231, F/G, STERILE |
Version Model Number | 8GA x 6" |
Catalog Number | RAN-86-14 |
Company DUNS | 121622872 |
Company Name | RANFAC CORP. |
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 | 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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 5085884400 |
info@ranfac.com |
Length | 6 Inch |
Length | 6 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857878007057 [Primary] |
GS1 | 10857878007054 [Package] Package: [1 Units] In Commercial Distribution |
GS1 | 20857878007051 [Package] Contains: 10857878007054 Package: [32 Units] In Commercial Distribution |
KNW | Instrument, Biopsy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-07-11 |
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