← Back to catalogue

Henso

FDA UDI

Class I (US FDA UDI)

by Henso Medical (Hangzhou) Co., Ltd.

Identity

Trade Name
Henso FDA UDI
Generic Name
Gastric pH strip FDA UDI
Model / Reference
PH Test Strips FDA UDI

Identifiers

Primary DI / UDI-DI
06970343581662 FDA UDI
FDA Product Code
LNW FDA UDI
GMDN Term
Gastric pH strip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1550 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

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

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: Gastric pH strip

Henso by Henso Medical (Hangzhou) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastric pH strip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 2b237d75-5df2-41f3-acff-5ce7afb0507f 32 fields · synced May 30, 2026