← Back to catalogue

Hl7

FDA UDI

Class I (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
HL7 FDA UDI
Generic Name
Clinical laboratory information system FDA UDI
Device Name
HL7 Forwarding Service Software FDA UDI
Model / Reference
Software, HL7 Forwarding Service - 3 FDA UDI
Description
HL7 Forwarding Service Software FDA UDI

Identifiers

Catalog Number
1104880 FDA UDI
Primary DI / UDI-DI
00606959039049 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Clinical laboratory information system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Clinical laboratory information system

Hl7 by Respironics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Clinical laboratory information system.

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
Respironics, Inc.

Sources (1)

  • FDA UDI a568662d-8af2-4d4d-a593-6e437ab79320 35 fields · synced Jun 8, 2026