Identity
- Trade Name
- Bard Button Device Decompression Tube FDA UDI
- Generic Name
- Gastrostomy tube FDA UDI
- Device Name
- 24 Fr x 1.7 Button Decompression Tube FDA UDI
- Model / Reference
- 000353 FDA UDI
- Description
- 24 Fr x 1.7 Button Decompression Tube FDA UDI
Identifiers
- Catalog Number
- 000353 FDA UDI
- Primary DI / UDI-DI
- 00801741080975 FDA UDI
- FDA Product Code
- KGC FDA UDI
- GMDN Term
- Gastrostomy tube FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
Dimensions & Sizes
- Size
- Catheter Gauge — 24 French FDA UDILength — 1.7 Centimeter FDA UDI
The Bard Button Device Decompression Tube is a medical device designed for patients with physical disabilities who require non-invasive enteral feeding or drainage of the stomach. This single-use, percutaneous tube decompresses the stomach and allows for safe delivery of nutrition or pharmaceutical agents.
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
- Bard Access Systems, Inc.
Sources (1)
- FDA UDI 31e6a4cf-94fb-471a-b5c4-ef4d9d010080 37 fields · synced Jul 11, 2026