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Code Rings

FDA UDI

Class I (US FDA UDI)

by Pulpdent Corporation

Identity

Trade Name
Code Rings FDA UDI
Generic Name
Surgical instrument track identification tape FDA UDI
Device Name
Silicone, medical grade. Box of 100 – white FDA UDI
Model / Reference
CR1 FDA UDI
Description
Silicone, medical grade. Box of 100 – white FDA UDI

Identifiers

Primary DI / UDI-DI
D701CR12 FDA UDI
FDA Product Code
EBL FDA UDI
GMDN Term
Surgical instrument track identification tape FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3740 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument track identification tape

Code Rings by Pulpdent Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument track identification tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0928dfe1-031c-483f-95aa-2237c14d99ff 33 fields · synced Jun 9, 2026