Identity
- Trade Name
- BodyMed FDA UDI
- Generic Name
- Patient medical adhesive remover FDA UDI
- Device Name
- BODYMED ADHESIVE REMOVER WIPE 1.6*3.2 INCH,50 PCS/BOX FDA UDI
- Model / Reference
- BDMARW50 FDA UDI
- Description
- BODYMED ADHESIVE REMOVER WIPE 1.6*3.2 INCH,50 PCS/BOX FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815991024771 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
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Patient medical adhesive remover
BodyMed by Boxout, Llc — 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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- ESENTA — CONVATEC, PURCHASING DEPARTMENT · Class I
- Sion Biotext Medical Ltd. — SION BIOTEXT MEDICAL LTD · Class I
- Adapt — Hollister Incorporated · Class I
- DETACHOL — Ferndale Laboratories, Inc. · Class I
- GluGone Adhesive Remover, 0.67 oz. — CHEMENCE MEDICAL INC. · 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
- Boxout, Llc
Sources (1)
- FDA UDI 22f40af6-7570-436a-91e6-4504acf2e7a5 33 fields · synced Jun 8, 2026