Identity
- Trade Name
- PDI® Adhesive Tape Remover Pad FDA UDI
- Generic Name
- Patient medical adhesive remover FDA UDI
- Device Name
- To remove adhesive tape from skin. FDA UDI
- Model / Reference
- B16400 FDA UDI
- Description
- To remove adhesive tape from skin. FDA UDI
Identifiers
- Catalog Number
- B16400 FDA UDI
- Primary DI / UDI-DI
- 00310819000451 FDA UDI
- FDA Product Code
- KOX FDA UDI
- GMDN Term
- Patient medical adhesive remover FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4730 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
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 1.2 Inch FDA UDIHeight — 2.6 Inch FDA UDI
Category: Patient medical adhesive remover
PDI® Adhesive Tape Remover Pad by Professional Disposables International, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Patient medical adhesive remover.
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- Adapt — Hollister Incorporated · Class I
- DETACHOL — Ferndale Laboratories, Inc. · Class I
- BodyMed — BOXOUT, LLC · Class I
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
- Professional Disposables International, Inc.
Sources (1)
- FDA UDI 6bf0f31c-d9e3-4c1f-bbb5-fd230102619a 36 fields · synced Jun 8, 2026