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Su-Veid

FDA UDI

Class II (US FDA UDI)

by Angie Technologies Ltd

Identity

Trade Name
SU-VEID FDA UDI
Generic Name
Invasive-detection multi-parameter physiological monitor, single-use FDA UDI
Device Name
Package of 30 SU-VEID units (DI# 07290018896037) FDA UDI
Model / Reference
18103200 FDA UDI
Description
Package of 30 SU-VEID units (DI# 07290018896037) FDA UDI

Identifiers

Catalog Number
18103200 FDA UDI
Primary DI / UDI-DI
07290018896136 FDA UDI
510(k) Number
K993995 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
Invasive-detection multi-parameter physiological monitor, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Invasive-detection multi-parameter physiological monitor, single-use

Su-Veid by Angie Technologies Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Invasive-detection multi-parameter physiological monitor, single-use.

Cleared under the same submission

K993995 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angie Technologies Ltd

Sources (1)

  • FDA UDI 56c6d7ba-fb2f-41c9-ac0c-1f83aa396620 35 fields · synced May 30, 2026