Identity
- Trade Name
- Pulset FDA UDI
- Generic Name
- Arterial blood sampling kit FDA UDI
- Device Name
- Pulset 3cc Syringe 23g x 1" (.6 x 25mm) Crickett 50u Balanced Heparin FDA UDI
- Model / Reference
- 3313-95 FDA UDI
- Description
- Pulset 3cc Syringe 23g x 1" (.6 x 25mm) Crickett 50u Balanced Heparin FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00709078006531 FDA UDI
- FDA Product Code
- CBT FDA UDI
- GMDN Term
- Arterial blood sampling kit FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.1100 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Pulset by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Westmed, Inc.
Sources (1)
- FDA UDI 37e053a4-ed42-452e-bd64-6c97f7c4f136 34 fields · synced Jun 6, 2026