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ESR rack for S-Sedivette®

FDA UDI

Class I (US FDA UDI)

by Sarstedt Aktiengesellschaft & Co.KG

Identity

Trade Name
ESR rack for S-Sedivette® FDA UDI
Generic Name
Erythrocyte sedimentation rate (ESR) rack IVD, scaled measure FDA UDI
Model / Reference
90.1090 FDA UDI

Identifiers

Catalog Number
90.1090 FDA UDI
Primary DI / UDI-DI
04038917085304 FDA UDI
FDA Product Code
JPH FDA UDI
GMDN Term
Erythrocyte sedimentation rate (ESR) rack IVD, scaled measure FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6700 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Erythrocyte sedimentation rate (ESR) rack IVD, scaled measure

ESR rack for S-Sedivette® by Sarstedt Aktiengesellschaft & Co.KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Erythrocyte sedimentation rate (ESR) rack IVD, scaled measure.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 973a8db3-f8cd-40f6-82a3-94051671e257 34 fields · synced May 30, 2026