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Propeller

FDA UDI

by Reciprocal Labs

Identity

Trade Name
Propeller FDA UDI
Generic Name
Inhaler dose sensor FDA UDI
Device Name
The convenience kit contains the following products: 2 x Propeller Sensor Model 2016-M-L (GTIN-14: 00865528000082) FDA UDI
Model / Reference
Convenience Kit - Mobile/SM2016ML/SM2016ML FDA UDI
Description
The convenience kit contains the following products: 2 x Propeller Sensor Model 2016-M-L (GTIN-14: 00865528000082) FDA UDI

Identifiers

Primary DI / UDI-DI
00859105006260 FDA UDI
GMDN Term
Inhaler dose sensor FDA UDI

Classification

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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Inhaler dose sensor

Propeller by Reciprocal Labs — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inhaler dose sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Reciprocal Labs

Sources (1)

  • FDA UDI 93c6cbfe-4cf1-480b-a61d-c4d8b3bca025 33 fields · synced Jun 8, 2026