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96" Pediatric Anesthesia Circuit

FDA UDI

Class I (US FDA UDI)

by Westmed, Inc.

Identity

Trade Name
96" Pediatric Anesthesia Circuit FDA UDI
Generic Name
Anaesthesia breathing circuit, single-use FDA UDI
Device Name
96" Pediatric Anesthesia Circuit, expandable, GSE w/Cap, Parallel Wye, GSL 10' x .050: ID M/M, 1L not made with latex breathing bag, B/V Filter (2), 14 French Oxygen Catheter FDA UDI
Model / Reference
9200 FDA UDI
Description
96" Pediatric Anesthesia Circuit, expandable, GSE w/Cap, Parallel Wye, GSL 10' x .050: ID M/M, 1L not made with latex breathing bag, B/V Filter (2), 14 French Oxygen Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
00709078009679 FDA UDI
510(k) Number
K922492 FDA UDI
FDA Product Code
OFP FDA UDI
CAH FDA UDI
GMDN Term
Anaesthesia breathing circuit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
868.5260 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia breathing circuit, single-use

96" Pediatric Anesthesia Circuit by Westmed, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Anaesthesia breathing circuit, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Westmed, Inc.

Sources (1)

  • FDA UDI 86900a86-7491-40b7-a821-67a630fbe5a7 34 fields · synced May 30, 2026