FDA UDI
Not in Commercial Distribution
🇺🇸 United States
CureWrap™ Pediatric 91-104cm (single)
DI: 07290107580199
·
Model: 500-03536
·
BELMONT INSTRUMENT CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Let the assistant research this device
The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.
Free to try · every answer cites its records
Basic Information
- Brand Name
- CureWrap™ Pediatric 91-104cm (single)
- Primary DI
- 07290107580199
- Version / Model
- 500-03536
- Catalog Number
- PED-L1001
- Company Name
- BELMONT INSTRUMENT CORPORATION
- Labeler DUNS
- 078330362
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2016-09-24
- Public Version
- 7
- Public Version Date
- 2026-04-14
- Public Version Status
- Update
- Public Device Record Key
- 0d204267-7a90-4922-967f-27973c8fed33
- Distribution End Date
- 2021-12-31
Device Description
Accessory for the CritiCool system.
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Unsafe
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| DWJ | System, Thermal Regulating | Cardiovascular | 870.5900 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 36956 | External circulating-fluid core temperature regulation system control unit, heating/cooling | An electrically-powered device intended to be used as part of an external circulating-fluid core temperature regulation system to control/regulate the temperature and flow of fluid through a connected patient-applied pad (not included), to both elevate and alternatively lower a patient’s core body temperature. The device includes a heater and refrigeration unit, a pump, and typically a water reservoir; it may also be intended for patient temperature monitoring and typically includes alarms for cases of water temperatures beyond pre-set limits. It is intended to be used by a healthcare professional in a clinical setting (e.g., to achieve normothermia). | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 07290107580199 | GS1 | ||||
| Package | 77290107580198 | GS1 | Box | 4 | Not in Commercial Distribution | 2021-12-31 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K083662 | 000 |