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T'Lift®

FDA UDI

Class I (US FDA UDI)

by Peters Surgical

Identity

Trade Name
T'Lift® FDA UDI
Generic Name
Externally-anchored laparoscopic retraction thread FDA UDI
Device Name
Single use, laparoscopic retraction system FDA UDI
Model / Reference
AW16280 FDA UDI
Description
Single use, laparoscopic retraction system FDA UDI

Identifiers

Catalog Number
AW16280 FDA UDI
Primary DI / UDI-DI
03700393301360 FDA UDI
FDA Product Code
NWV FDA UDI
GMDN Term
Externally-anchored laparoscopic retraction thread FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Externally-anchored laparoscopic retraction thread

T'Lift® by Peters Surgical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Externally-anchored laparoscopic retraction thread.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Peters Surgical

Sources (1)

  • FDA UDI 72f81a58-ca81-435d-bcab-69714727fb5a 35 fields · synced May 29, 2026