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EndoRotor® Specimen Trap (Single)

FDA UDI

Class II (US FDA UDI)

by Interscope, Inc

Identity

Trade Name
EndoRotor® Specimen Trap (Single) FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Model / Reference
ER 30-01 FDA UDI

Identifiers

Catalog Number
ER 30-01 FDA UDI
Primary DI / UDI-DI
00865830000244 FDA UDI
FDA Product Code
PTE FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.1690 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

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

Yes

FDA UDI

Category: Surgical suction system collection container, single-use

EndoRotor® Specimen Trap (Single) by Interscope, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Interscope, Inc

Sources (1)

  • FDA UDI f0a04054-471f-4a4a-b5d5-fda36aae72e9 34 fields · synced May 30, 2026