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ERPeak

FDA UDI

Class I (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
ERPeak FDA UDI
Generic Name
General specimen container IVD, additive/medium FDA UDI
Device Name
IVD Sample kit FDA UDI
Model / Reference
ER20190829-04 FDA UDI
Description
IVD Sample kit FDA UDI

Identifiers

Primary DI / UDI-DI
60888937027190 FDA UDI
FDA Product Code
NNK FDA UDI
GMDN Term
General specimen container IVD, additive/medium FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: General specimen container IVD, additive/medium

ERPeak by CooperSurgical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, additive/medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a087770f-ff6b-41cd-bcc5-66ed024117d5 33 fields · synced Jun 9, 2026