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Exhaust Collection Bag

FDA UDI

Class III (US FDA UDI)

by Channel Medsystems, Inc.

Identity

Trade Name
Exhaust Collection Bag FDA UDI
Generic Name
General cryosurgical system, cryogen gas, electronic FDA UDI
Device Name
Single exhaust collection bag in pouch FDA UDI
Model / Reference
FGS-7005 FDA UDI
Description
Single exhaust collection bag in pouch FDA UDI

Identifiers

Primary DI / UDI-DI
00850008595028 FDA UDI
PMA Number
P180032 FDA UDI
FDA Product Code
MNB FDA UDI
GMDN Term
General cryosurgical system, cryogen gas, electronic FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Exhaust Collection Bag by Channel Medsystems, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d8b2c460-d55a-4dfd-b004-47bba345dbb1 36 fields · synced Jun 6, 2026