Cordguard®
- Primary DI
- H671CRD2011
- Brand
- Cordguard®
- Company
- UTAH MEDICAL PRODUCTS, INC.
- Model
- II
- Catalog number
- CRD-201
- Device description
- Disposable umbilical cord clamp, cut, and blood collection device.
- Published
- 2017-06-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KNA | Instrument, Manual, Specialized Obstetric-Gynecologic |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KNA | Instrument, Manual, Specialized Obstetric-Gynecologic | Obstetrics/Gynecology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K954619 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| H671CRD2011 | Package | HIBCC | 10 | In Commercial Distribution |
| H671CRD2010 | Primary | HIBCC | 0 |
GMDN Terms#
| Term | Definition |
|---|---|
| Umbilical cord blood collection set | A group of devices intended to be used to collect, process, and store umbilical cord blood and/or umbilical cord blood components (e.g., buffy coat). It typically includes tubing, hollow needles for insertion into the umbilical cord (a double venipuncture of the cord) to collect the blood, and several containers (flexible bags usually containing an anticoagulant) intended for transitional (room temperature) or long-term (frozen) blood storage. The cord blood is usually intended to be frozen and stored, typically to preserve stem cells, for subsequent reinfusion into patients, generally in cases of leukaemia. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| 800-533-4984 | customer@utahmed.com |
Regulatory Flags#
- DUNS number
- 094651270
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- true
- 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
- true
- Sterilization required before use
- false
Other Devices From This Company#
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|---|---|---|---|---|
| H671303TT0 | CMI | Tender Touch Cup | 303TT | 2016-09-23 |
| H671303TTL0 | CMI | Tender Touch Cup | 303TTL | 2016-09-23 |
| H671404TT0 | CMI | Tender Touch Cup | 404TT | 2016-09-23 |
| H67141828050 | UMBILI-CATH | Single-Lumen Polyurethane | 4182805 | 2016-09-23 |
| H67141835050 | UMBILI-CATH | Single-Lumen Polyurethane | 4183505 | 2016-09-23 |
| H67141850050 | UMBILI-CATH | Single-Lumen Polyurethane | 4185005 | 2016-09-23 |
| H67141865050 | UMBILI-CATH | Single-Lumen Polyurethane | 4186505 | 2016-09-23 |
| H67142828050 | UMBILI-CATH | Dual-Lumen Polyurethane | 4282805 | 2016-09-23 |
| H67142835050 | UMBILI-CATH | Dual-Lumen Polyurethane | 4283505 | 2016-09-23 |
| H67142850050 | UMBILI-CATH | Dual-Lumen Polyurethane | 4285005 | 2016-09-23 |
| H67143850050 | UMBILI-CATH | Triple-Lumen Polyurethane | 4385005 | 2016-09-23 |
| H671444FC0 | CMI | Flex Cup | 444FC | 2016-09-23 |
| H671505TT0 | CMI | Ultra Cup | 505TT | 2016-09-23 |
| H671505TTL0 | CMI | Ultra Cup | 505TTL | 2016-09-23 |
| H671506TTL0 | CMI | Ultra Cup | 506TTL | 2016-09-23 |
| H671600TT0 | CMI | Secure Cup | 600TT | 2016-09-23 |
| H671606TT0 | CMI | Secure Cup | 606TT | 2016-09-23 |
| H671IUP4000 | INTRAN | Plus | IUP-400 | 2016-09-23 |
| H671IUP4500 | INTRAN | Plus | IUP-450 | 2016-09-23 |
| H671IUP5000 | INTRAN | Plus | IUP-500 | 2016-09-23 |
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