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Spirovit Sp-250

FDA UDI

Class II (US FDA UDI)

by Schiller Corp.

Identity

Trade Name
SPIROVIT SP-250 FDA UDI
Generic Name
Diagnostic spirometer, professional FDA UDI
Device Name
The SPIROVIT SP-250 spirometer is used together with the plastic mouth piece to conduct slow and forced spirometry maneuvers. FDA UDI
Model / Reference
2.200560 FDA UDI
Description
The SPIROVIT SP-250 spirometer is used together with the plastic mouth piece to conduct slow and forced spirometry maneuvers. FDA UDI

Identifiers

Catalog Number
2.200560 FDA UDI
Primary DI / UDI-DI
07613365000108 FDA UDI
510(k) Number
K984031 FDA UDI
FDA Product Code
BZG FDA UDI
GMDN Term
Diagnostic spirometer, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1840 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

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: Diagnostic spirometer, professional

Spirovit Sp-250 by Schiller Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Diagnostic spirometer, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schiller Corp.

Sources (1)

  • FDA UDI f39b2e5d-f103-441b-b47e-7e78a51b77c2 37 fields · synced Jun 1, 2026