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Adapter, Rubber, 1 3/8 TO 7/8

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 113600Model Reusable Rubber Mouthpiece and Components

by A-M Systems, Inc.

Identity

Trade Name
Rubber Adapter EUDAMED
Adapter, Rubber, 1 3/8 TO 7/8 FDA UDI
Generic Name
Breathing mouthpiece, reusable FDA UDI
Device Name
Reusable Rubber Mouthpiece and Components EUDAMED
Adapter, Tube, Blue Autoclavable Thermoplastic Rubber, 1 3/8 TO 7/8 FDA UDI
Model / Reference
Reusable Rubber Mouthpiece and Components EUDAMED
113600 EUDAMED
Adapter, Rubber, 1 3/8 TO 7/8 - 113600 FDA UDI
Description
Adapter, Tube, Blue Autoclavable Thermoplastic Rubber, 1 3/8 TO 7/8 FDA UDI

Identifiers

Catalog Number
113600 FDA UDI
Primary DI / UDI-DI
00817081022865 EUDAMEDFDA UDI
Basic UDI-DI
081708102164XXXLF EUDAMED
FDA Product Code
BYP FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Breathing mouthpiece, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5620 FDA UDI
Market of Registration
Bulgaria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breathing mouthpiece, reusable

Adapter, Rubber, 1 3/8 TO 7/8 by A-M Systems, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Breathing mouthpiece, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
A-M Systems, Inc.

Sources (2)

  • FDA UDI ea1e3f5f-85eb-4247-ab13-ad243344916d 35 fields · synced Jul 25, 2026
  • EUDAMED 166ee222-b79a-487e-8eb6-d2b40248130f 61 fields · synced Jul 25, 2026