Identity
- Trade Name
- RECEPTAL™ Floor Suction Device FDA UDI
- Generic Name
- Suction system canister liner FDA UDI
- Device Name
- RECEPTAL™ Floor Suction Device Pole and hook for floor suction disc FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- RECEPTAL™ Floor Suction Device Pole and hook for floor suction disc FDA UDI
Identifiers
- Catalog Number
- FSK001 FDA UDI
- Primary DI / UDI-DI
- 40704411011720 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
- 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
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: Suction system canister liner
RECEPTAL™ Floor Suction Device by Amsino International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Suction system canister liner.
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- Pergo — PERGO MEDIKAL VE ILAC SANAYI ANONIM SIRKETI · Class II
- DeRoyal — PERGO MEDIKAL VE ILAC SANAYI ANONIM SIRKETI · Class II
- Suction Liner — Shijiazhuang Yuanding Medical Device Co., LTD · 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
- Amsino International, Inc.
Sources (1)
- FDA UDI 19fe5a1b-f084-4b0f-9157-6f532b02a745 34 fields · synced Jun 8, 2026