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Pc

FDA UDI

Class I (US FDA UDI)

by Allied Medical LLC

Identity

Trade Name
PC FDA UDI
Generic Name
Carbon dioxide absorbent FDA UDI
Device Name
LITHOLYME,GEMULTISTYLE,6/CS FDA UDI
Model / Reference
55-01-0017 FDA UDI
Description
LITHOLYME,GEMULTISTYLE,6/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00026072025260 FDA UDI
FDA Product Code
CBL FDA UDI
GMDN Term
Carbon dioxide absorbent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5300 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Carbon dioxide absorbent

Pc by Allied Medical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Carbon dioxide absorbent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Allied Medical LLC

Sources (1)

  • FDA UDI 3889856a-c518-4443-8ff6-6d040ade5ab1 33 fields · synced Jun 1, 2026