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Disposable Bulb & Bladder

FDA UDI

Class I (US FDA UDI)

by Healthmark Industries Co., Inc.

Identity

Trade Name
Disposable Bulb & Bladder FDA UDI
Generic Name
Endoscope inflation bulb FDA UDI
Model / Reference
D30200-210 FDA UDI

Identifiers

Catalog Number
D30200-210 FDA UDI
Primary DI / UDI-DI
10848956005291 FDA UDI
FDA Product Code
FCY FDA UDI
GMDN Term
Endoscope inflation bulb FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscope inflation bulb

Disposable Bulb & Bladder by Healthmark Industries Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope inflation bulb.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 272f9b80-6c1c-43f8-888e-fb5656e5339c 34 fields · synced May 30, 2026