← Back to catalogue

CareTouch

FDA UDI

Class I (US FDA UDI)

by Carelife (usa) Inc.

Identity

Trade Name
CareTouch FDA UDI
Generic Name
ENFit oral/enteral syringe, single-use FDA UDI
Device Name
10ml oral tip FDA UDI
Model / Reference
1 FDA UDI
Description
10ml oral tip FDA UDI

Identifiers

Catalog Number
CTSOS10 FDA UDI
Primary DI / UDI-DI
M992CTSOS10100B3 FDA UDI
FDA Product Code
KYX FDA UDI
GMDN Term
ENFit oral/enteral syringe, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6430 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: ENFit oral/enteral syringe, single-use

CareTouch by Carelife (usa) Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENFit oral/enteral syringe, single-use.

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
Carelife (usa) Inc.

Sources (1)

  • FDA UDI 56f083b5-7602-40cc-9ae1-58f5847da1c0 35 fields · synced Jun 6, 2026