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Fenestrated Circumcision Drape

FDA UDI

Class II (US FDA UDI)

by Standard Textile Co., Inc.

Identity

Trade Name
Fenestrated Circumcision Drape FDA UDI
Generic Name
Patient surgical drape, reusable FDA UDI
Device Name
Circumcision Drape, 55% cotton/45% polyester 1 Ply Standard Supreme, 1 ply Barrier Supreme Reinforcement pad on back of drape, w 1" round fenestration, concealed hems around fenestration and reinforcement, hemmed all around, 12x12 FDA UDI
Model / Reference
96201672 FDA UDI
Description
Circumcision Drape, 55% cotton/45% polyester 1 Ply Standard Supreme, 1 ply Barrier Supreme Reinforcement pad on back of drape, w 1" round fenestration, concealed hems around fenestration and reinforcement, hemmed all around, 12x12 FDA UDI

Identifiers

Catalog Number
96201672 FDA UDI
Primary DI / UDI-DI
00634916418187 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Patient surgical drape, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
Not 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Fenestrated Circumcision Drape by Standard Textile Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Standard Textile Co., Inc.

Sources (1)

  • FDA UDI 468f143e-5382-46b2-886e-8759eedd0a2d 36 fields · synced May 30, 2026