Identity
- Trade Name
- GluGone Adhesive Remover, 2 oz. FDA UDI
- Generic Name
- Patient medical adhesive remover FDA UDI
- Device Name
- Glugone 2 oz FDA UDI
- Model / Reference
- GG80212 FDA UDI
- Description
- Glugone 2 oz FDA UDI
Identifiers
- Catalog Number
- GG80212 FDA UDI
- Primary DI / UDI-DI
- 00854137001719 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Patient medical adhesive remover
GluGone Adhesive Remover, 2 oz. by Chemence Medical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Patient medical adhesive remover.
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- 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
- Chemence Medical Inc.
Sources (1)
- FDA UDI 51219bce-8be6-42b7-b407-f1f1877f558a 35 fields · synced Sep 18, 2026