Primary Device ID | 04546951525484 |
NIH Device Record Key | e150fcd2-c004-4ff3-8b8a-0fb55550969a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MANI Sutures PGA |
Version Model Number | 404 |
Catalog Number | 404 |
Company DUNS | 690622428 |
Company Name | MANI, 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 | 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 | 04546951525484 [Primary] |
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 | 3 |
Public Version Date | 2018-07-09 |
Device Publish Date | 2016-03-25 |
04546951525514 | 503 |
04546951525507 | 502 |
04546951525491 | 501 |
04546951525484 | 404 |
04546951525477 | 403 |
04546951525460 | 402 |
04546951525453 | 401 |
04546951525446 | 303 |
04546951525439 | 302 |
04546951525422 | 301 |
14546951404366 | MANI Ophthalmic Sutures |
14546951403833 | MANI Ophthalmic Sutures |
14546951403802 | MANI Ophthalmic Sutures |
14546951403666 | MANI Ophthalmic Sutures |
04546951403201 | MANI Ophthalmic Sutures |
04546951403195 | MANI Ophthalmic Sutures |
04546951403188 | MANI Ophthalmic Sutures |
04546951403171 | MANI Ophthalmic Sutures |
04546951403164 | MANI Ophthalmic Sutures |
04546951403140 | MANI Ophthalmic Sutures |