| Primary Device ID | 37613327405591 |
| NIH Device Record Key | f2c8e4d9-e6f2-4263-90dc-afc8f048e254 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SurgiCount Safety-Sponge |
| Version Model Number | 0601008360 |
| Catalog Number | 0601008360 |
| Company DUNS | 196548481 |
| Company Name | STRYKER CORPORATION |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com | |
| Phone | +1(800)253-3210 |
| Inst.Stryker.cs@Stryker.com |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Length | 36 Inch |
| Width | 8 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327405590 [Primary] |
| GS1 | 37613327405591 [Package] Contains: 07613327405590 Package: pack [160 Units] In Commercial Distribution |
| GDY | GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
[37613327405591]
Radiation Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2025-09-04 |
| Device Publish Date | 2018-09-24 |