| Primary Device ID | 10612376000101 |
| NIH Device Record Key | 61c98a6a-0487-4eb9-b762-e4371db6876b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Count-Tainer 20 |
| Version Model Number | 5120F |
| Company DUNS | 005245386 |
| Company Name | ANCHOR PRODUCTS COMPANY |
| 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 |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com | |
| Phone | 800-323-5134 |
| info@anchorsurgical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00612376000104 [Primary] |
| GS1 | 10612376000101 [Package] Contains: 00612376000104 Package: [20 Units] In Commercial Distribution |
| MMK | Container, Sharps |
| 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 | 2016-09-19 |
| 00612376000135 | 5120FNS |
| 10612376000101 | 5120F |