HEMOVAC® 00-1509-014-10
GUDID 00889024370258
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable Closed-wound drain, non-bioabsorbable| Primary Device ID | 00889024370258 |
| NIH Device Record Key | edb76e53-546c-4334-907d-04e5733b995d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HEMOVAC® |
| Version Model Number | 00-1509-014-10 |
| Catalog Number | 00-1509-014-10 |
| Company DUNS | 137354267 |
| Company Name | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 |
Customer Support Contacts
Device Dimensions
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 4.8 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024370258 [Primary] |
FDA Product Code
| GCY | Apparatus, Suction, Single Patient Use, Portable, Nonpowered |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-02-23 |
| Device Publish Date | 2020-09-23 |
Devices Manufactured by ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.
| 00889024616325 - Stablecut® | 2024-04-17 |
| 00889024616332 - Stablecut® | 2024-04-17 |
| 00889024626447 - A.T.S.® Personalized Pressure® | 2023-09-07 |
| 00889024647497 - Stablecut® | 2023-03-03 |
| 00889024647503 - Stablecut® | 2023-03-03 |
| 00889024647510 - Stablecut® | 2023-03-03 |
| 00889024647527 - Stablecut® | 2023-03-03 |
| 00889024647534 - Stablecut® | 2023-03-03 |
Trademark Results [HEMOVAC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 HEMOVAC 74536475 1901660 Live/Registered |
ZIMMER, INC 1994-06-13 |
 HEMOVAC 73502743 1473000 Dead/Cancelled |
SNYDER LABORATORIES INC. 1984-10-09 |
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