Identity
- Trade Name
- Full Power AED FDA UDI
- Generic Name
- Hypoallergenic skin adhesive tape FDA UDI
- Device Name
- Adhesive Medical Device to remove chest hair before defibrillation FDA UDI
- Model / Reference
- Rapid Hair Removal Pads FDA UDI
- Description
- Adhesive Medical Device to remove chest hair before defibrillation FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00867855000308 FDA UDI
- 510(k) Number
- K150349 FDA UDI
- FDA Product Code
- LDD FDA UDI
- GMDN Term
- Hypoallergenic skin adhesive tape FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Width — 5.872 Inch FDA UDIHeight — 7.95 Inch FDA UDI
Category: Hypoallergenic skin adhesive tape
Full Power AED by Full Power Aed — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Hypoallergenic skin adhesive tape.
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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
- Full Power Aed
Sources (1)
- FDA UDI 542a3ebe-64b0-4e2f-be2a-0e2b727f3064 36 fields · synced Jun 1, 2026