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Lansinoh

FDA UDI

Class I (US FDA UDI)

by Pigeon Industries (thailand) Company Limited

Identity

Trade Name
LANSINOH FDA UDI
Generic Name
Nipple shielding teat, reusable FDA UDI
Device Name
Sterile Nipple Shield FDA UDI
Model / Reference
70195 FDA UDI
Description
Sterile Nipple Shield FDA UDI

Identifiers

Primary DI / UDI-DI
00044677701952 FDA UDI
FDA Product Code
HGY FDA UDI
GMDN Term
Nipple shielding teat, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Nipple shielding teat, reusable

Lansinoh by Pigeon Industries (thailand) Company Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nipple shielding teat, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3f54307b-27ea-493d-b350-0ea9eace67cf 33 fields · synced Jun 1, 2026