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Schiller NIBP cuff

FDA UDI

Class II (US FDA UDI)

by Schiller Corp.

Identity

Trade Name
Schiller NIBP cuff FDA UDI
Generic Name
Blood pressure cuff, reusable FDA UDI
Device Name
NIBP cuff luer lock 25 to 35 cm FDA UDI
Model / Reference
2.120026 FDA UDI
Description
NIBP cuff luer lock 25 to 35 cm FDA UDI

Identifiers

Catalog Number
2.120026 FDA UDI
Primary DI / UDI-DI
07613365000566 FDA UDI
510(k) Number
K012226 FDA UDI
FDA Product Code
DXQ FDA UDI
GMDN Term
Blood pressure cuff, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1120 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Blood pressure cuff, reusable

Schiller NIBP cuff by Schiller Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood pressure cuff, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Schiller Corp.

Sources (1)

  • FDA UDI 7f1565b8-b785-4036-8b49-bfe5bd87ef31 37 fields · synced Jun 8, 2026