Identity
- Trade Name
- DALTON WET WIPE FDA UDI
- Generic Name
- Skin cleaning wipe FDA UDI
- Device Name
- WET WIPE, UNSCENT, 7.9"X12", 48/PK FDA UDI
- Model / Reference
- IN-AWP100 FDA UDI
- Description
- WET WIPE, UNSCENT, 7.9"X12", 48/PK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815027010303 FDA UDI
- FDA Product Code
- LRJ FDA UDI
- GMDN Term
- Skin cleaning wipe FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6890 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
Category: Skin cleaning wipe
Dalton Wet Wipe by Dalton Medical Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin cleaning wipe.
- SAPS Health alcohol pads — HOME AIDE DIAGNOSTICS, INC. · U
- CSD — CHINA SURGICAL DRESSINGS CENTER CO., LTD. · U
- Easy Comfort Alcohol Pads 50 count — HOME AIDE DIAGNOSTICS, INC. · U
- Curaplex — BOUND TREE MEDICAL, LLC · Class I
- Safety 1st — DOREL JUVENILE GROUP, INC. · Class I
- REMI — Epitel, Inc. · Class II
- Pro Comfort Alcohol Pads — HOME AIDE DIAGNOSTICS, INC. · U
- Easy Comfort Alcohol Pads — HOME AIDE DIAGNOSTICS, INC. · U
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dalton Medical Corp.
Sources (1)
- FDA UDI 22390376-ee7f-4fe4-b937-4d9075c9e8d8 33 fields · synced Jun 8, 2026