Identity
- Trade Name
- EXEL HIS ROTATING WING, NON-DEHP W/Y 22GX3/4" FDA UDI
- Generic Name
- Subcutaneous infusion/injection port needle FDA UDI
- Device Name
- EXEL HIS ROTATING WING, NON-DEHP W/Y 22GX3/4", 25/INNERBX, 50/BX, 20BX/CRTN FDA UDI
- Model / Reference
- 27949R FDA UDI
- Description
- EXEL HIS ROTATING WING, NON-DEHP W/Y 22GX3/4", 25/INNERBX, 50/BX, 20BX/CRTN FDA UDI
Identifiers
- Catalog Number
- 27949R FDA UDI
- Primary DI / UDI-DI
- 00020221079494 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- Subcutaneous infusion/injection port needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- Commercial Distribution
- 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
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Subcutaneous infusion/injection port needle
Exel His Rotating Wing, Non-Dehp W/Y 22gx3/4" by Exel International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Exel International
Sources (1)
- FDA UDI 5d8ea076-4d2d-4d46-b64c-ed33a221ff97 35 fields · synced May 30, 2026