Primary Device ID | B160211827P1 |
NIH Device Record Key | 80390fb5-534a-4496-98eb-767b78ea7f03 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Procedure Products Needles |
Version Model Number | 21-1827-P |
Company DUNS | 151507563 |
Company Name | PROCEDURE PRODUCTS, INC. |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B160211827P1 [Primary] |
DRE | Dilator, Vessel, For Percutaneous Catheterization |
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 | 2017-09-27 |
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B1603293552 | 19ga, 1-wall needle |
B160311827P1 | NEEDLE, W/O BASEPLATE 7CM 18g W/ PLUG |
B1603118151 | NEEDLES, W/O BASEPLATE 3.8CM 18g |
B1602293572 | 19ga, 7cm, 1-part needle |
B1602118352 | NEEDLE, BSDN PLATE 1 PART 9 CM 18g |
B160211827P1 | 18 GA needle, 7cm, BSDN, with Plug |
B1602018401 | NEEDLE, 2 PART, 10.2cm, 18g, MODIFIED POTTS |
B1602018221 | Needle, 18ga, 5.7cm, 2-part |