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Conmed

FDA UDI

Class II (US FDA UDI)

by Unimax Medical Systems Inc.

Identity

Trade Name
CONMED FDA UDI
Generic Name
Tissue extraction bag FDA UDI
Device Name
Endo Pouch FDA UDI
Model / Reference
SB1036 FDA UDI
Description
Endo Pouch FDA UDI

Identifiers

Primary DI / UDI-DI
04714127860657 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Tissue extraction bag FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tissue extraction bag

Conmed by Unimax Medical Systems Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue extraction bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ad72ed7a-10a7-4d34-868b-ec3ec3eb2ef3 33 fields · synced Jun 8, 2026