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Baramed

FDA UDI

Class II (US FDA UDI)

by Perry Baromedical Corporation

Identity

Trade Name
Baramed FDA UDI
Generic Name
Hyperbaric chamber, stationary FDA UDI
Device Name
Baramed 30 Monoplace Hyperbaric Chamber FDA UDI
Model / Reference
Baramed 30 FDA UDI
Description
Baramed 30 Monoplace Hyperbaric Chamber FDA UDI

Identifiers

Primary DI / UDI-DI
00852678007122 FDA UDI
510(k) Number
K993010 FDA UDI
FDA Product Code
CBF FDA UDI
GMDN Term
Hyperbaric chamber, stationary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5470 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hyperbaric chamber, stationary

Baramed by Perry Baromedical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hyperbaric chamber, stationary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Perry Baromedical Corporation

Sources (1)

  • FDA UDI 588a8ea4-31dd-4a82-82e3-ebff611e2522 34 fields · synced Jun 9, 2026