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Conta-Guard

FDA UDI

Class I (US FDA UDI)

by Rønvig Dental Manufacturing A/S

Identity

Trade Name
CONTA-GUARD FDA UDI
Generic Name
Needle recapping device, single-use FDA UDI
Device Name
200 pcs. of laminated disposable foil for protection against needle stick. FDA UDI
Model / Reference
2200 FDA UDI
Description
200 pcs. of laminated disposable foil for protection against needle stick. FDA UDI

Identifiers

Primary DI / UDI-DI
05713513000089 FDA UDI
FDA Product Code
BRW FDA UDI
GMDN Term
Needle recapping device, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5820 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

No

FDA UDI

Over-the-Counter

Yes

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: Needle recapping device, single-use

Conta-Guard by Rønvig Dental Manufacturing A/S — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needle recapping device, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rønvig Dental Manufacturing A/S

Sources (1)

  • FDA UDI 313b6ca0-5862-4bf3-8102-c23868c947f7 33 fields · synced May 31, 2026