Identity
- Trade Name
- Bemis FDA UDI
- Generic Name
- Suction system canister liner FDA UDI
- Device Name
- 1500CC QUICKFIT LINER 50 PACK INDIVIDUALLY BAGGED FDA UDI
- Model / Reference
- 1504 FDA UDI
- Description
- 1500CC QUICKFIT LINER 50 PACK INDIVIDUALLY BAGGED FDA UDI
Identifiers
- Catalog Number
- 1504 FDA UDI
- Primary DI / UDI-DI
- 10073088149210 FDA UDI
- 510(k) Number
- K771737 FDA UDI
- FDA Product Code
- GCX FDA UDI
- GMDN Term
- Suction system canister liner FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Dimensions & Sizes
- Size
- Total Volume — 1500 Milliliter FDA UDI
Bemis by Bemis de México, S.A. de C.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K771737 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 |
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Manufacturer
- Manufacturer
- Bemis de México, S.A. de C.V.
Sources (1)
- FDA UDI d66e48c2-602d-4534-b0fd-53dcb250ce2d 38 fields · synced May 30, 2026