Primary Device ID | 10848782022622 |
NIH Device Record Key | 7db16c27-1937-4948-8409-2cd7fbeae81f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dsm19 4-0 Vio Mnd 18"/45cm |
Version Model Number | YP-513N |
Catalog Number | YP-513 |
Company DUNS | 812762226 |
Company Name | Surgical Specialties México, S. de R.L. de C.V. |
Device Count | 1 |
DM Exempt | true |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00848782022625 [Primary] |
GS1 | 10848782022622 [Package] Contains: 00848782022625 Package: Box [12 Units] In Commercial Distribution |
GAM | SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-22 |
10848782022622 | Dsm19 4-0 Vio Mnd 18"/45cm |
10848782021458 | Dsm19 4-0 Vio Mnd 18"/45cm |