Identity
- Trade Name
- Sklar® FDA UDI
- Generic Name
- Kick bucket FDA UDI
- Device Name
- HOSPITAL BUCKET 13QT W/O LID FDA UDI
- Model / Reference
- 10-1182 FDA UDI
- Description
- HOSPITAL BUCKET 13QT W/O LID FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10649111290268 FDA UDI
- FDA Product Code
- FSM FDA UDI
- GMDN Term
- Kick bucket FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Kick bucket
Sklar® by Sklar Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Kick bucket.
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class I
- Carnegie Surgical LLC — Carnegie Surgical LLC · Class I
- HYGITECH — HYGITECH · Class I
- Sklar — Sklar Corporation · Class I
- Sklar® — Sklar Corporation · Class I
- Sklar® — Sklar Corporation · Class I
- Sklar® — Sklar Corporation · Class I
- Sklar® — Sklar Corporation · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sklar Corporation
Sources (1)
- FDA UDI aaa69e52-1635-4078-ad4c-f3f4bdc4d74b 33 fields · synced May 30, 2026