Primary Device ID | 00616784340128 |
NIH Device Record Key | b8034a59-b3a8-471e-ad8c-82f9dc0f19d6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Packing Strip |
Version Model Number | 3401 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
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 | false |
Serial Number | false |
Manufacturing Date | false |
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 | 00616784340128 [Primary] |
GS1 | 00616784340135 [Package] Package: Case [12 Units] In Commercial Distribution |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-03 |
Device Publish Date | 2022-04-25 |
00616784340425 | Packing Strip, Plain, Sterile, 2" x 5 yd. (50.08 mm x 4.6 m) |
00616784340326 | Packing Strip, Plain, Sterile, 1" x 5 yd. (25.4mm x 4.6m) |
00616784340227 | Packing Strip, Plain, Sterile, 1/2" x 5 yd. (13mm x 4.6m) |
00616784340128 | Packing Strip, Plain, Sterile, 1/4" x 5 yd. (6mm x 4.6m) |