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seca 217

FDA UDI

Class I (US FDA UDI)

by Seca Corp.

Identity

Trade Name
seca 217 FDA UDI
Generic Name
Patient-height measure FDA UDI
Device Name
The mobile stadiometer seca 217 boasts unmatched stability, a cleverly designed assembly system and particularly high-quality materials. All this lends the stadiometer an exceptionally high degree of stability – almost the same as a permanent installation. In addition, the adjustable spacer ensures a secure hold without any fittings. Suitable for medical practices and hospitals, the stadiometer is also just right for mobile use, such as examinations of children at school or patients at home. When disassembled, the stadiometer is easy to carry anywhere. FDA UDI
Model / Reference
217 FDA UDI
Description
The mobile stadiometer seca 217 boasts unmatched stability, a cleverly designed assembly system and particularly high-quality materials. All this lends the stadiometer an exceptionally high degree of stability – almost the same as a permanent installation. In addition, the adjustable spacer ensures a secure hold without any fittings. Suitable for medical practices and hospitals, the stadiometer is also just right for mobile use, such as examinations of children at school or patients at home. When disassembled, the stadiometer is easy to carry anywhere. FDA UDI

Identifiers

Catalog Number
2171821009 FDA UDI
Primary DI / UDI-DI
04012030008938 FDA UDI
FDA Product Code
FRW FDA UDI
GMDN Term
Patient-height measure FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2720 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Patient-height measure

seca 217 by Seca Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient-height measure.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Seca Corp.

Sources (1)

  • FDA UDI 71427768-7020-4802-83c4-35612e3307b8 35 fields · synced May 30, 2026