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Connector refill, Careshield

FDA UDI

Class I (US FDA UDI)

by J.H. Orsing AB

Identity

Trade Name
Connector refill, Careshield FDA UDI
Generic Name
Dental suction system cannula, single-use FDA UDI
Device Name
Careshield FDA UDI
Model / Reference
Careshield FDA UDI
Description
Careshield FDA UDI

Identifiers

Catalog Number
CN5 FDA UDI
Primary DI / UDI-DI
07393507592028 FDA UDI
FDA Product Code
EHZ FDA UDI
GMDN Term
Dental suction system cannula, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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: Dental suction system cannula, single-use

Connector refill, Careshield by J.H. Orsing AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental suction system cannula, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
J.H. Orsing AB

Sources (1)

  • FDA UDI 1c270714-8e2c-4766-8a0c-cb9ba7571fe0 34 fields · synced Jun 1, 2026