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Centurion

FDA UDI

Class I (US FDA UDI)

by Centurion Medical Products

Identity

Trade Name
Centurion FDA UDI
Generic Name
Infant blanket, reusable FDA UDI
Device Name
STERILE BABY BLANKET FDA UDI
Model / Reference
80017ST FDA UDI
Description
STERILE BABY BLANKET FDA UDI

Identifiers

Catalog Number
80017ST FDA UDI
Primary DI / UDI-DI
10653160244714 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Infant blanket, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 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: Infant blanket, reusable

Centurion by Centurion Medical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Infant blanket, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Centurion Medical Products

Sources (1)

  • FDA UDI 13e99ad2-be21-4b5e-ab8a-515c772d9229 35 fields · synced May 30, 2026