StayFIX®
- Primary DI
- 10884450023355
- Brand
- StayFIX®
- Company
- Merit Medical Systems, Inc.
- Model
- 00884450023358
- Catalog number
- 680ME/C
- Published
- 2018-02-16
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- false
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes#
| Code | Name |
|---|---|
| KGX | Tape and bandage, adhesive |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KGX | Tape And Bandage, Adhesive | General Hospital | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 10884450023355 | Package | GS1 | 25 | In Commercial Distribution |
| 20884450023352 | Package | GS1 | 16 | In Commercial Distribution |
| 00884450023358 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 10884450023355 | 10884450023355 | ||
| 20884450023352 | 20884450023352 | ||
| 00884450023358 | 00884450023358 | 884450023358 | 0884450023358 |
GMDN Terms#
| Term | Definition |
|---|---|
| Anaesthesia conduction catheter holder, sterile | A sterile device in the form of an adhesive backed pad with a locking mechanism that is used to secure an anaesthesia conduction catheter at the skin insertion site to prevent catheter migration. Also known as an epidural securement device. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Sterilization Methods#
| Method |
|---|
Regulatory Flags#
- DUNS number
- 184763290
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00884450392898 | SCOUT MD™ | Initial Release | MDS10A-01 | 2026-05-23 |
| 00884450392904 | SCOUT MD™ | Initial Release | MDS10B-01 | 2026-05-23 |
| 00884450392911 | SCOUT MD™ | Initial Release | MDS10C-01 | 2026-05-23 |
| 00884450393383 | SCOUT MD™ | Initial Release | MDS75SA-01 | 2026-05-23 |
| 00884450399965 | SCOUT MD™ | Initial Release | MDS75SM-01 | 2026-05-23 |
| 00884450435120 | Merit Medical® | Initial Release | K09-10345A | 2026-05-22 |
| 00884450435533 | Merit Medical® | Initial Release | K07-00112C | 2026-05-23 |
| 00884450437049 | Merit Medical® | Initial Release | K11-01136C | 2026-05-23 |
| 00884450437162 | Merit Medical® | Initial Release | K09-10786C | 2026-05-22 |
| 00884450441350 | Merit Medical® | Initial Release | K09-14004B | 2026-05-23 |
| 00884450474587 | Merit Medical® | Initial Release | K12T-12714 | 2026-05-23 |
| 10884450029364 | Merit Medical® | Initial Release | K08-02142B | 2026-03-24 |
| 10884450111731 | Merit Medical® | Initial Release | K09-11186D | 2026-03-24 |
| 00884450220696 | Merit Medical® | Initial Release | K05T-02138B | 2026-03-24 |
| 10884450423629 | Merit Medical® | Initial Release | K09-13891B | 2026-03-24 |
| 10884450425333 | Merit Medical® | Initial Release | K10-01481A | 2026-03-24 |
| 20884450430815 | Merit Medical® | Initial Release | K09-05342B | 2026-03-24 |
| 10884450430863 | Merit Medical® | Initial Release | K09-10929A | 2026-03-24 |
| 00884450458426 | DuraMax® | B | H787103028225 | 2026-03-24 |
| 10884450529581 | SplashWire™ | Initial Release | MSWSTFS35220 | 2026-03-24 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00628942588907 | Blistape | Blistape Inc | KGX | 2026-03-10 |
| 00628942588983 | Blistape | Blistape Inc | KGX | 2026-03-10 |
| 60041260026852 | Kroger | KROGER CO., THE | KGX | 2026-03-09 |
| 00819143026354 | Healqu | Healqu LLC | KGX | 2026-03-05 |
| 00819143026453 | Healqu | Healqu LLC | KGX | 2026-03-05 |
| 00861092002644 | Cealogic Film | RECIBIO, INC. | KGX | 2026-03-01 |
| 50192253049815 | Telfa | Cardinal Health 200, LLC | KGX | 2026-02-25 |
| 50192253050088 | Telfa | Cardinal Health 200, LLC | KGX | 2026-02-25 |
| 30197344181654 | CURAD | MEDLINE INDUSTRIES, INC. | KGX | 2026-02-23 |
| 00819143026309 | Healqu | Healqu LLC | KGX | 2026-02-19 |
| 05715205000360 | Plum QuickFix | Plum Safety ApS | KGX | 2026-02-17 |
| 05715205000407 | Plum QuickFix | Plum Safety ApS | KGX | 2026-02-17 |
| 05715205000438 | Plum QuickFix | Plum Safety ApS | KGX | 2026-02-17 |
| 05715205000469 | Plum QuickFix | Plum Safety ApS | KGX | 2026-02-17 |
| 05715205100015 | Plum QuickSoft | Plum Safety ApS | KGX | 2026-02-17 |
| 05715205110014 | Plum QuickSoft | Plum Safety ApS | KGX | 2026-02-17 |
| 05715205120013 | Plum QuickSoft | Plum Safety ApS | KGX | 2026-02-17 |
| 00197998014789 | Solventum™ Transpore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998014871 | Solventum™ Transpore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998018916 | Solventum™ Transpore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998018978 | Solventum™ Transpore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998021985 | Solventum™ Medipore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998023590 | Solventum™ Transpore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998023750 | Solventum™ Medipore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998023781 | Solventum™ Medipore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998023811 | Solventum™ Medipore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998025891 | Solventum™ Medipore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998028052 | Solventum™ Micropore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998028090 | Solventum™ Micropore™ | Solventum US LLC | KGX | 2026-02-15 |
| 00197998028410 | Solventum™ Micropore™ | Solventum US LLC | KGX | 2026-02-15 |