Identity
- Trade Name
- basixCOMPAK™ FDA UDI
- Generic Name
- Catheter/overtube balloon inflator, single-use FDA UDI
- Model / Reference
- 00884450535134 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884450535134 FDA UDI
- FDA Product Code
- PTM FDA UDI
- GMDN Term
- Catheter/overtube balloon inflator, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1650 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
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: Catheter/overtube balloon inflator, single-use
basixCOMPAK™ by Merit Medical Systems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Catheter/overtube balloon inflator, single-use.
- GENOSS Inflator B40 — Genoss · Class II
- AngioDynamics — NAVILYST MEDICAL, INC.
- NuVent™ — MEDTRONIC XOMED, INC. · Class I
- QL Disposable Inflation Device — Atrion Medical Products, Inc. · Class II
- Mannequin™ Endoventricular Shaper — KDL MEDICAL, INC. · Class II
- AngioDynamics — NAVILYST MEDICAL, INC.
- Encore 40 Inflation Device — Atrion Medical Products, Inc. · Class II
- GM-30 Inflation Device — Infraredx, 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
- Merit Medical Systems, Inc.
Sources (1)
- FDA UDI 47a0b337-3de9-4406-8c76-c1960ea4b3fb 32 fields · synced Jun 9, 2026