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Measurement Forcep, Handle Type like master sample, Follow master sample and cus

FDA UDI

Class I (US FDA UDI)

by Iaa Surgical Instruments Company

Identity

Trade Name
Measurement Forcep, Handle Type like master sample, Follow master sample and cus FDA UDI
Generic Name
Bronchoscopic biopsy curette, flexible, reusable FDA UDI
Model / Reference
BPS2006 FDA UDI

Identifiers

Catalog Number
BPS2006 FDA UDI
Primary DI / UDI-DI
B832BPS20060 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Bronchoscopic biopsy curette, flexible, reusable 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

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

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

No

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

Category: Bronchoscopic biopsy curette, flexible, reusable

Measurement Forcep, Handle Type like master sample, Follow master sample and cus by Iaa Surgical Instruments Company — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Bronchoscopic biopsy curette, flexible, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 59d9a894-b42b-4529-b89d-cd5fd298af79 33 fields · synced May 30, 2026