← Back to catalogue

Polyester Tape

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
Polyester Tape FDA UDI
Generic Name
Surgical support tape, non-bioabsorbable FDA UDI
Device Name
Braided Polyester,Pre-Cut,2x White Strands FDA UDI
Model / Reference
88868618-00 FDA UDI
Description
Braided Polyester,Pre-Cut,2x White Strands FDA UDI

Identifiers

Primary DI / UDI-DI
10884521104440 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Surgical support tape, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 30 Inch FDA UDI

Category: Surgical support tape, non-bioabsorbable

Polyester Tape by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical support tape, non-bioabsorbable.

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
Covidien LP

Sources (1)

  • FDA UDI 5c349449-cc06-4991-8fee-d636ae5dc690 35 fields · synced May 31, 2026