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Esperance

FDA UDI

Class II (US FDA UDI)

by Shanghai Wallaby Medical Technologies Co., Inc.

Identity

Trade Name
Esperance FDA UDI
Generic Name
Thrombectomy suction catheter FDA UDI
Device Name
Thrombectomy suction catheter FDA UDI
Model / Reference
ASP5F131KIT FDA UDI
Description
Thrombectomy suction catheter FDA UDI

Identifiers

Primary DI / UDI-DI
06970908211850 FDA UDI
FDA Product Code
NRY FDA UDI
GMDN Term
Thrombectomy suction catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Thrombectomy suction catheter

Esperance by Shanghai Wallaby Medical Technologies Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thrombectomy suction catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shanghai Wallaby Medical Technologies Co., Inc.

Sources (1)

  • FDA UDI 20d6f055-2a9c-4864-83e5-c781cda298ec 33 fields · synced May 30, 2026