← Back to catalogue

lovtec

FDA UDI

Class I (US FDA UDI)

by Danyang Airtech Co., Ltd.

Identity

Trade Name
lovtec FDA UDI
Generic Name
Hyperbaric chamber, stationary FDA UDI
Device Name
Reduce the gas cylinder outlet pressure. FDA UDI
Model / Reference
AT15 FDA UDI
Description
Reduce the gas cylinder outlet pressure. FDA UDI

Identifiers

Primary DI / UDI-DI
06978311830002 FDA UDI
FDA Product Code
CAN FDA UDI
GMDN Term
Hyperbaric chamber, stationary FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.2700 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hyperbaric chamber, stationary

lovtec by Danyang Airtech Co., Ltd. — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Danyang Airtech Co., Ltd.

Sources (1)

  • FDA UDI 89c2b762-ab4f-4529-bf00-f23ec1f6054b 33 fields · synced May 30, 2026