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RECEPTAL™ Suction Procedure Kit

FDA UDI

Class II (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
RECEPTAL™ Suction Procedure Kit FDA UDI
Generic Name
Suction system canister liner FDA UDI
Device Name
RECEPTAL™ Suction Procedure Kit EZE-VAC® Disposable Canister with lid, elbows on patient and vacuum port Non-sterile suction tube 3/16 in. ID × 6 ft. (5 mm × 1.8 m) with connnectors Non-sterile suction tube 3/16 in. ID × 18 ft. (5 mm × 46 cm) with connnectors FDA UDI
Model / Reference
1 FDA UDI
Description
RECEPTAL™ Suction Procedure Kit EZE-VAC® Disposable Canister with lid, elbows on patient and vacuum port Non-sterile suction tube 3/16 in. ID × 6 ft. (5 mm × 1.8 m) with connnectors Non-sterile suction tube 3/16 in. ID × 18 ft. (5 mm × 46 cm) with connnectors FDA UDI

Identifiers

Catalog Number
ELID2-820821 FDA UDI
Primary DI / UDI-DI
10704411011521 FDA UDI
FDA Product Code
KDQ 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

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: Suction system canister liner

RECEPTAL™ Suction Procedure Kit by Amsino International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction system canister liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0886390a-6da3-492a-b5d0-e827ee5f7cea 34 fields · synced Jun 1, 2026