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SteriTec 1" Green Tape

FDA UDI

Class II (US FDA UDI)

by Steritec Product Mfg. Co., Inc.

Identity

Trade Name
SteriTec 1" Green Tape FDA UDI
Generic Name
Sterilization packaging tape FDA UDI
Model / Reference
CI 159/1, CI 165/1 FDA UDI

Identifiers

Catalog Number
CI 159/1, CI 165/1 FDA UDI
Primary DI / UDI-DI
00814434020189 FDA UDI
510(k) Number
K122555 FDA UDI
FDA Product Code
JOJ FDA UDI
GMDN Term
Sterilization packaging tape FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.2800 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Sterilization packaging tape

SteriTec 1" Green Tape by Steritec Product Mfg. Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sterilization packaging tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 419a2349-dd0a-4e95-b06f-2e1842358d42 35 fields · synced Jun 8, 2026