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Receptal™ Liner

FDA UDI

Class II (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
RECEPTAL™ LINER FDA UDI
Generic Name
General-purpose suction system, vacuum FDA UDI
Device Name
RECEPTAL™ LINER FDA UDI
Model / Reference
1 FDA UDI
Description
RECEPTAL™ LINER FDA UDI

Identifiers

Catalog Number
430423001 FDA UDI
Primary DI / UDI-DI
20704411000041 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
General-purpose suction system, vacuum 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: General-purpose suction system, vacuum

Receptal™ Liner by Amsino International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose suction system, vacuum.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Amsino International, Inc.

Sources (1)

  • FDA UDI 5e01325d-6f26-43f7-8c2b-5db6514b52bc 34 fields · synced Jun 1, 2026