Identity
- Trade Name
- Bard® Ellik Evacuator FDA UDI
- Generic Name
- Bladder evacuator, single-use FDA UDI
- Device Name
- Bard® Ellik Evacuator FDA UDI
- Model / Reference
- 000451 FDA UDI
- Description
- Bard® Ellik Evacuator FDA UDI
Identifiers
- Catalog Number
- 000451 FDA UDI
- Primary DI / UDI-DI
- 00801741080814 FDA UDI
- FDA Product Code
- KQT FDA UDI
- GMDN Term
- Bladder evacuator, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.4370 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
Yes
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
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: Bladder evacuator, single-use
Bard® Ellik Evacuator by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bladder evacuator, single-use.
- Tur Vac — ALLWIN MEDICAL DEVICES, INC. · Class II
- Ellik Bladder Evacuator — C. R. Bard, Inc. · Class II
- Bard® Ellik Bladder Evacuator (Reservoir Only) — C. R. Bard, Inc. · Class II
- Bard® Ellik Bladder Evacuator — C. R. Bard, Inc. · Class II
- Bladder Evacuator — C. R. Bard, Inc. · Class II
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 |
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Manufacturer
- Manufacturer
- C. R. Bard, Inc.
Sources (1)
- FDA UDI 5bc0fcfd-e37e-4e50-8890-99b0f82d992c 35 fields · synced Jun 8, 2026