Identity
- Trade Name
- SNAP™ FDA UDI
- Generic Name
- Dry skin moisture barrier dressing FDA UDI
- Device Name
- Snap Securring hydrocolloid FDA UDI
- Model / Reference
- Snap Securring FDA UDI
- Description
- Snap Securring hydrocolloid FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00849554006362 FDA UDI
- 510(k) Number
- K132080 FDA UDI
- FDA Product Code
- OKO FDA UDI
- GMDN Term
- Dry skin moisture barrier dressing FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4683 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
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Dry skin moisture barrier dressing
Snap™ by Kci Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K132080 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Kci Usa, Inc.
Sources (1)
- FDA UDI 011014b9-4885-4572-80ec-1b426c0d4ecc 34 fields · synced May 30, 2026